U.S. patent application number 15/034543 was filed with the patent office on 2016-12-01 for novel methods.
This patent application is currently assigned to Aeromics, Inc.. The applicant listed for this patent is AEROMICS, INC.. Invention is credited to George William FARR, Paul Robert MCGUIRK, Marc F. PELLETIER, Steven WILLIAMS.
Application Number | 20160346302 15/034543 |
Document ID | / |
Family ID | 53042097 |
Filed Date | 2016-12-01 |
United States Patent
Application |
20160346302 |
Kind Code |
A1 |
PELLETIER; Marc F. ; et
al. |
December 1, 2016 |
NOVEL METHODS
Abstract
The present invention relates to the use of selective aquaporin
inhibitors, e.g., of aquaporin-4 or aquaporin-2, e.g., certain
phenylbenzamide compounds, for the prophylaxis, treatment and
control of aquaporin-mediated conditions, e.g., glioblastoma and
ovarian hyperstimulation syndrome. The invention provides, inter
alia, methods of treating or controlling a disease condition
mediated by an aquaporin, e.g., diseases or conditions of water
imbalance and other diseases.
Inventors: |
PELLETIER; Marc F.; (Shaker
Heights, OH) ; MCGUIRK; Paul Robert; (Spring Hill,
FL) ; FARR; George William; (Rocky River, OH)
; WILLIAMS; Steven; (Columbus, OH) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
AEROMICS, INC. |
Cleveland |
OH |
US |
|
|
Assignee: |
Aeromics, Inc.
Cleveland
OH
|
Family ID: |
53042097 |
Appl. No.: |
15/034543 |
Filed: |
November 6, 2014 |
PCT Filed: |
November 6, 2014 |
PCT NO: |
PCT/US2014/064432 |
371 Date: |
May 4, 2016 |
Related U.S. Patent Documents
|
|
|
|
|
|
Application
Number |
Filing Date |
Patent Number |
|
|
61900878 |
Nov 6, 2013 |
|
|
|
61900946 |
Nov 6, 2013 |
|
|
|
61900919 |
Nov 6, 2013 |
|
|
|
Current U.S.
Class: |
1/1 |
Current CPC
Class: |
A61P 15/00 20180101;
A61P 7/00 20180101; A61P 25/08 20180101; A61P 35/00 20180101; A61P
7/08 20180101; A61P 9/00 20180101; C07F 9/09 20130101; A61K 31/222
20130101; A61P 1/16 20180101; A61P 25/06 20180101; A61P 11/00
20180101; A61K 31/5375 20130101; A61P 9/10 20180101; A61K 31/661
20130101; A61P 31/04 20180101; A61K 31/167 20130101; A61K 9/0019
20130101; A61P 25/00 20180101; A61P 21/00 20180101; A61P 7/10
20180101; A61P 43/00 20180101; A61P 27/02 20180101; A61P 9/04
20180101; A61K 47/18 20130101 |
International
Class: |
A61K 31/661 20060101
A61K031/661; A61K 31/167 20060101 A61K031/167 |
Claims
1. A method of treating or controlling a disease or condition
mediated by an aquaporin comprising administering to a patient in
need thereof an effective amount of a phenylbenzamide inhibitor of
aquaporin, wherein the condition to be treated or controlled is
glioblastoma, ovarian hyperstimulation syndrome, pulmonary edema,
fibromyalgia, or multiple sclerosis.
2. A method according to claim 1 wherein the phenylbenzamide is a
compound of Formula I: ##STR00013## wherein X represents a
connecting group whose number of atoms in the main chain is 2 to 5
(said connecting group may be substituted), A represents a hydrogen
atom or an acyl group which may be substituted, or a C.sub.1 to
C.sub.6 alkyl group which may be substituted, or A may bind to
connecting group X to form a cyclic structure which may be
substituted, E represents an aryl group which may be substituted or
a heteroaryl group which may be substituted, ring Z represents an
arene which may have one or more substituents in addition to the
group represented by formula --O-A wherein A has the same meaning
as that defined above and the group represented by formula --X-E
wherein each of X and E has the same meaning as that defined above,
or a heteroarene which may have one or more substituents in
addition to the group represented by formula --O-A wherein A has
the same meaning as that defined above and the group represented by
formula --X-E wherein each of X and E has the same meaning as that
defined above; in free or pharmaceutically acceptable salt
form.
3. The method of claim 2 wherein the compound of Formula I is
selected from the compounds of formula (I) described in US
2010/0274051 A1, the compounds of formula (I) as described in U.S.
Pat. No. 7,700,655, and the compounds of formula (I) as described
in U.S. Pat. No. 7,626,042.
4. The method of claim 3 wherein the compound of Formula I is
selected from Compound Nos. 1-223 in US 2010/0274051 A1, Compound
Nos. 301-555 in U.S. Pat. No. 7,700,655, and Compound Nos. 1-151 in
U.S. Pat. No. 7,626,042.
5. The method of claim 2 wherein the compound of Formula I is a
compound of formula 1a: ##STR00014## wherein R.sub.1, R.sub.2,
R.sub.3, R.sub.4, and R.sub.5 are selected from H, halo,
halogenated C.sub.1-4 alkyl, and cyano; and R.sub.6 is selected
from H and physiologically hydrolysable and acceptable acyl; in
free or pharmaceutically acceptable salt form.
6. The method of claim 5 wherein R.sub.1 is selected from
trifluoromethyl, chloro, fluoro, and bromo; R.sub.3 and R.sub.5 are
the same or different and selected from trifluoromethyl, chloro,
fluoro, and bromo; and R.sub.2 and R.sub.4 are both H.
7. The method of claim 6 wherein R.sub.1 is selected from chloro
and bromo; R.sub.3 and R.sub.5 are both trifluoromethyl; and
R.sub.2, R.sub.4 and R.sub.6 are all H.
8. The method of claim 5 or 6 wherein R.sub.6 is H.
9. The method of claim 5 or 6 wherein R.sub.6 is acetyl.
10. The method of claim 8 wherein R.sub.1 is selected from chloro
and bromo; R.sub.3 and R.sub.5 are both trifluoromethyl; and
R.sub.2 and R.sub.4 are H; and R.sub.6 is acetyl.
11. The method of claim 7 wherein R.sub.1 is chloro.
12. The method of claim 6 wherein R.sub.1, R.sub.3 and R.sub.5 are
each chloro, and R.sub.2, R.sub.4 and R.sub.6 are each H.
13. The method of claim 6 wherein R.sub.1, R.sub.3 and R.sub.5 are
each trifluoromethyl, and R.sub.2, R.sub.4 and R.sub.6 are each
H.
14. The method of claim 5 or 6 wherein R.sub.6 is C.sub.1-4
acyl.
15. The method of claim 5 or 6 wherein R.sub.6 is the residue of an
amino acid.
16. The method of claim 5 or 6 wherein R.sub.6 is a 5 to 6-membered
non-aromatic heterocyclic ring-carbonyl group, for example a 5 to
6-membered non-aromatic heterocyclic ring-carbonyl group which
comprises at least one nitrogen atom as ring-constituting atoms
(ring forming atoms) of said heterocyclic ring and binds to the
carbonyl group at the nitrogen atom, e.g., wherein said 5 to
6-membered non-aromatic heterocyclic ring is selected from
1-pyrrolidinyl group, piperidino group, morpholino group, and
1-piperazinyl group, and said heterocyclic ring may be substituted
with one or more substituents, e.g., independently selected from an
alkyl group, an alkyl-oxy-carbonyl group, and a carboxy group; for
example wherein R.sub.6 is (morpholin-4-yl)carbonyl.
17. The method of claim 5 or 6 wherein R.sub.6 is a
N,N-di-substituted carbamoyl group, wherein two substituents of
said carbamoyl group may combine to each other, together with the
nitrogen atom to which they bind, to form a nitrogen-containing
heterocyclic group which may be substituted.
18. The method of claim 5 or 6 wherein R.sub.6 is a
(morpholin-4-yl)carbonyl group.
19. The method of claim 5 or 6 wherein R.sub.6 is a phosphono
group, which may be substituted, e.g. dibenzylphosphono, or
unsubstituted.
20. The method of claim 1 wherein the phenylbenzamide is
niclosamide.
21. The method of claim 1 or 5 wherein the phenylbenzamide is
selected from ##STR00015## ##STR00016##
22. The method of claim 1 or 5 wherein the phenylbenzamide is
##STR00017##
23. The method of claim 1 or 5 wherein the phenylbenzamide is
##STR00018##
24. The method of any of the foregoing claims wherein the condition
to be treated or controlled is glioblastoma.
25. The method of any of claims 1-23 wherein the condition to be
treated or controlled is ovarian hyperstimulation syndrome.
26. The method of any of the foregoing claims wherein the condition
to be treated or controlled is pulmonary edema.
27. The method of any of the foregoing claims wherein the condition
to be treated or controlled is fibromyalgia.
28. The method of any of the foregoing claims wherein the condition
to be treated or controlled is multiple sclerosis.
29. Use of a phenylbenzamide, e.g. niclosamide or a compound of
Formula I or formula 1a as hereinbefore described, in the
manufacture of a medicament for treating or controlling a disease
or condition mediated by an aquaporin, e.g., for use in any of the
methods of claims 1-28.
30. A pharmaceutical composition comprising a phenylbenzamide, e.g.
niclosamide or a compound of Formula I or formula 1a as
hereinbefore described, in combination with a pharmaceutically
acceptable diluent or carrier for use in any of the methods of
claims 1-28.
31. A method of treating or controlling glioblastoma comprising
administering an effective amount of an inhibitor of AQP4, e.g, a
compound binding to AQP4, e.g., a phenylbenzamide, e.g.,
niclosamide or a compound of Formula I or formula 1a, e.g., a
compound of claims 1-23, to a patient in need thereof.
32. A method of treating or controlling ovarian hyperstimulation
syndrome comprising administering an effective amount of an
aquaporin inhibitor, e.g., a phenylbenzamide, e.g., niclosamide or
a compound of Formula I or formula 1a, e.g., a compound of claims
1-23, to a patient in need thereof.
33. A method of treating or controlling pulmonary edema comprising
administering an effective amount of an inhibitor of AQP4, e.g, a
compound binding to AQP4, e.g., a phenylbenzamide, e.g.,
niclosamide or a compound of Formula I or formula 1a, e.g., a
compound of claims 1-23, to a patient in need thereof.
34. A method of treating or controlling fibromyalgia comprising
administering an effective amount of an inhibitor of AQP4, e.g, a
compound binding to AQP4, e.g., a phenylbenzamide, e.g.,
niclosamide or a compound of Formula I or formula 1a, e.g., a
compound of claims 1-23, to a patient in need thereof.
35. A method of treating or controlling multiple sclerosis
comprising administering an effective amount of an inhibitor of
AQP4, e.g, a compound binding to AQP4, e.g., a phenylbenzamide,
e.g., niclosamide or a compound of Formula I or formula 1a, e.g., a
compound of claims 1-23, to a patient in need thereof.
36. A method of treating or controlling glioblastoma comprising
administering to a patient in need thereof an aquaporin inhibitor,
e.g., a phenylbenzamide, e.g., niclosamide or a compound of Formula
I or formula 1a, e.g., a compound of claims 1-23, in an amount
effective to inhibit the aquaporin.
37. A method of treating or controlling ovarian hyperstimulation
syndrome comprising administering to a patient in need thereof an
aquaporin inhibitor, e.g., a phenylbenzamide, e.g., niclosamide or
a compound of Formula I or formula 1a, e.g., a compound of claims
1-23, in an amount effective to inhibit the aquaporin.
38. A method of treating or controlling pulmonary edema comprising
administering to a patient in need thereof an aquaporin inhibitor,
e.g., a phenylbenzamide, e.g., niclosamide or a compound of Formula
I or formula 1a, e.g., a compound of claims 1-23, in an amount
effective to inhibit the aquaporin.
39. A method of treating or controlling fibromyalgia comprising
administering to a patient in need thereof an aquaporin inhibitor,
e.g., a phenylbenzamide, e.g., niclosamide or a compound of Formula
I or formula 1a, e.g., a compound of claims 1-23, in an amount
effective to inhibit the aquaporin.
40. A method of treating or controlling multiple sclerosis
comprising administering to a patient in need thereof an aquaporin
inhibitor, e.g., a phenylbenzamide, e.g., niclosamide or a compound
of Formula I or formula 1a, e.g., a compound of claims 1-23, in an
amount effective to inhibit the aquaporin.
41. A method to inhibit an aquaporin in a patient suffering from
glioblastoma comprising administering an effective amount of an
aquaporin inhibitor, e.g., a phenylbenzamide, e.g. niclosamide or a
compound of Formula I or formula 1a, e.g., a compound of claims
1-23, in an amount effective to inhibit the aquaporin.
42. A method to inhibit an aquaporin in a patient suffering from
ovarian hyperstimulation syndrome comprising administering an
effective amount of an aquaporin inhibitor, e.g., a
phenylbenzamide, e.g. niclosamide or a compound of Formula I or
formula 1a, e.g., a compound of claims 1-23, in an amount effective
to inhibit the aquaporin.
43. A method to inhibit an aquaporin in a patient suffering from
pulmonary edema comprising administering an effective amount of an
aquaporin inhibitor, e.g., a phenylbenzamide, e.g. niclosamide or a
compound of Formula I or formula 1a, e.g., a compound of claims
1-23, in an amount effective to inhibit the aquaporin.
44. A method to inhibit an aquaporin in a patient suffering from
fibromyalgia comprising administering an effective amount of an
aquaporin inhibitor, e.g., a phenylbenzamide, e.g. niclosamide or a
compound of Formula I or formula 1a, e.g., a compound of claims
1-23, in an amount effective to inhibit the aquaporin.
45. A method to inhibit an aquaporin in a patient suffering from
multiple sclerosis comprising administering an effective amount of
an aquaporin inhibitor, e.g., a phenylbenzamide, e.g. niclosamide
or a compound of Formula I or formula 1a, e.g., a compound of
claims 1-23, in an amount effective to inhibit the aquaporin.
Description
FIELD OF THE INVENTION
[0001] The present invention relates to the use of selective
aquaporin inhibitors, e.g., of aquaporin-4 or aquaporin-2, e.g.,
certain phenylbenzamide compounds, for the prophylaxis, treatment
and control of aquaporin-mediated conditions, e.g., glioblastoma
and ovarian hyperstimulation syndrome or, e.g., pulmonary edema,
fibromyalgia, and multiple sclerosis.
BACKGROUND OF THE INVENTION
[0002] Aquaporins are cell membrane proteins that act as molecular
water channels to mediate the flow of water in and out of the
cells. While there is some degree of passive diffusion or osmosis
of water across cell membranes, the rapid and selective transport
of water in and out of cells involves aquaporins. These water
channels selectively conduct water molecules in and out of the
cell, while blocking the passage of ions and other solutes, thereby
preserving the membrane potential of the cell. Aquaporins are found
in virtually all life forms, from bacteria to plants to animals. In
humans, they are found in cells throughout the body.
[0003] Cerebral edema (CE) is a major contributor to stroke damage,
as it can result in increased intracerebral pressure (ICP), a
corresponding decrease in cerebral perfusion, and potentially
permanent or fatal brain damage. Edema also contributes to CNS
damage in, for example, traumatic brain and spinal cord injury,
glioma, meningitis, acute mountain sickness, epileptic seizures,
infections, metabolic disorders, hypoxia, water intoxication,
hepatic failure, hepatic encephalopathy, diabetic ketoacidosis,
abscess, eclampsia, Creutzfeldt-Jakob disease, and lupus
cerebritis. Patients surviving the period of maximal ICP, usually
the three days following a stroke or traumatic brain injury, are
likely to survive. Unfortunately, only a few treatment options are
available for CE, and these are of limited efficacy.
[0004] Hyponatremia, characterized by serum sodium levels
.ltoreq.135 mM, is the most common form of electrolyte imbalance
with hospitals nationwide reporting an incidence of 15-20%. The
associated fluid retention is symptomatic of heart failure (HF),
liver cirrhosis, nephrotic disorder, and syndrome of inappropriate
antidiuretic hormone secretion (SIADH). Various diuretics are used
to treat congestion associated with HF. By inhibiting the Na/K/Cl
cotransporter in the thick ascending loop of Henle, loop diuretics
cause natriuresis by decreasing Na.sup.+ and Cl.sup.- reabsorption
from the urine. An alternative therapy for hyponatremia is the use
of vasopressin receptor antagonists, which inhibit water
reabsorption by inhibiting the vasopressin-induced trafficking of
AQP2. Unfortunately, both loop diuretics and vasopressin receptor
antagonists act indirectly toward a desired physiological outcome.
An ideal drug would block water reabsorption directly, thus
minimizing potential side-effects caused by upstream effectors, but
no such drugs are currently known.
[0005] Epilepsy is a brain disorder characterized by recurrent
seizures. Seizures occur because of disturbed brain activity
resulting in some degree of temporary brain dysfunction. Seizures
may cause uncontrollable shaking and loss of consciousness but,
more commonly, a person experiencing a seizure stops moving or
becomes unaware of what is happening. Anticonvulsants may be used
to treat epilepsy, however anticonvulsants are not effective for
all people with epilepsy.
[0006] AQP4 inhibitors may be of further utility for certain
ailments where control of AQP4-medited water movement may augment
neuroexcitation (by alteration of neuronal potassium homeostasis)
and prove beneficial by reducing neuronal excitation, for example
in ailments such as fibromyalgia, multiple sclerosis, migraines and
seizures (in particular but not limited to seizures associated with
epilepsy).
[0007] Ischemia is a condition characterized by an interruption or
inadequate supply of blood to tissues. Retinal ischemia occurs due
to a deficient supply of blood to the retina. Vascular occlusion,
glaucoma, and diabetic retinopathy are associated with retinal
ischemia and can produce retinal edema and ganglion cell death
leading to visual impairment and blindness. AQP4 is expressed in
the Muller cells in the retina. Due to relatively ineffectual
treatment, retinal ischemia remains a common cause of visual
impairment and blindness.
[0008] Myocardial ischemia is a condition caused by a blockage or
constriction of one more of the coronary arteries, such as can
occur with atherosclerotic plaque occlusion or rupture. Myocardial
infarction, a heart attack, occurs when myocardial ischemia exceeds
a critical threshold and overwhelms myocardial cellular repair
mechanisms designed to maintain normal operating function and
homeostasis. Myocardial infarction remains a leading cause of
morbidity and mortality worldwide. Compounds effective in treating
myocardial ischemia, myocardial ischemia/reperfusion injury,
myocardial infarction, and congestive heart failure would be useful
pharmaceuticals.
[0009] Phenylbenzamide compounds are known as pharmaceuticals.
Phenylbenzamides include compounds such niclosamide
(5-chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide), an
antihemintic agent used to treat tapeworms, but are not known to
have any effect on aquaporins. US Patent Publication US
2010/0274051 A1 (the contents of which are incorporated herein by
reference) describe certain phenylbenzamides as being useful to
inhibit NF-.kappa.B via selective inhibition of IKK-.beta., while
U.S. Pat. No. 7,626,042 (also incorporated herein by reference)
discloses O-acyl derivatives of such compounds, while U.S. Pat. No.
7,700,655 (also incorporated herein by reference) describe certain
phenylbenzamides as being useful to treat allergic diseases. These
patent applications, however, do not disclose anything about
cerebral edema or water imbalance (aquaresis) or aquaporins.
[0010] In a 2004 paper, a group purportedly investigated the
efficacy of
N-(3,5-Bis-trifluoromethyl-phenyl)-5-chloro-2-hydroxy-benzamide in
I.kappa.B phosphorylation blockade in a rat myocardial
ischemia/reperfusion injury model. Onai, Y. et al., "Inhibition of
I.kappa.B Phosphorylation in Cardiomyocytes Attenuates Myocardial
Ischemia/Reperfusion Injury," Cardiovascular Research, 2004, 63,
51-59. The group reported some activity. However, subsequently, the
activity effect could not be confirmed and accordingly
N-(3,5-Bis-trifluoromethyl-phenyl)-5-chloro-2-hydroxy-benzamide was
not pursued for this indication in humans.
[0011] Prior to this invention, there are have been no known
specific, validated inhibitors of aquaporins, for example AQP4 or
AQP2. Certain antiepileptic or sulfonamide drugs (e.g.,
acetylsulfanilamide, acetazolamide,
6-ethoxy-benzothiazole-2-sulfonamide, topiramate, zonisamide,
phenytoin, lamotrigine, and sumatriptan) were at one point reported
to be possible inhibitors of AQP4, but this later proved to be
incorrect. Yang, et al., Bioorganic & Medicinal Chemistry
(2008) 16: 7489-7493. No direct inhibitors of AQP2 have been
reported. The search for therapeutically useful aquaporin
inhibitors has been hampered by a lack of effective high throughput
screening assays, as well as by a lack of highly selective
inhibitors to develop and validate the assays and to serve as
positive controls or binding competitors.
[0012] There is a great need for improved approaches to treating
and controlling diseases of water imbalance, such as edema, for
example cerebral edema, and water retention and hyponatremia, as
well as diseases such as epilepsy, retinal ischemia, myocardial
ischemia, myocardial ischemia/reperfusion injury, myocardial
infarction, myocardial hypoxia, congestive heart failure, sepsis,
and neuromyelitis optica, as well as migraines.
BRIEF SUMMARY OF THE INVENTION
[0013] The invention provides the use of selective aquaporin
inhibitors, e.g., of aquaporin-4 or aquaporin-2 for the
prophylaxis, treatment and control of aquaporin-mediated
conditions, e.g., diseases of water imbalance, for example edema
(particularly edema of the brain and spinal cord, e.g., following
trauma or ischemic stroke, as well as the edema associated with
glioma, meningitis, acute mountain sickness, epileptic seizures,
infections, metabolic disorders, water intoxication, hepatic
failure, hepatic encephalopathy, diabetic ketoacidosis, abscess,
eclampsia, Creutzfeldt-Jakob disease, and lupus cerebritis, as well
as the edema consequent to microgravity and/or radiation exposure,
as well as edema consequent to invasive central nervous system
procedures, e.g., neurosurgery, endovascular clot removal, spinal
tap, aneurysm repair, or deep brain stimulation, as well as retinal
edema, as well as brain swelling consequent to cardiac arrest,
e.g., related to the development of the metabolic acidosis (e.g.
lactic acidosis) due to hypoxia before the resuscitation period),
as well as hyponatremia and excess fluid retention, as well as
ovarian hyperstimulation syndrome, as well as diseases such as
epilepsy, retinal ischemia and other diseases of the eye associated
with abnormalities in intraocular pressure or tissue hydration,
myocardial ischemia, myocardial ischemia/reperfusion injury,
myocardial infarction, myocardial hypoxia, congestive heart
failure, sepsis, neuromyelitis optica, and glioblastoma, as well as
migraines.
[0014] The invention further provides the use of certain
phenylbenzamides to inhibit aquaporins, particularly AQP4 and
AQP2.
[0015] The invention provides, inter alia, methods of treating or
controlling a disease or condition mediated by an aquaporin, e.g.,
diseases or conditions of water imbalance and other diseases, for
example, [0016] edema of the brain or spinal cord, e.g., cerebral
edema, e.g. cerebral edema consequent to head trauma, ischemic
stroke, glioma, meningitis, acute mountain sickness, epileptic
seizures, infections, metabolic disorders, hypoxia (including
general systemic hypoxia and hypoxia due to cardiac arrest), water
intoxication, hepatic failure, hepatic encephalopathy, diabetic
ketoacidosis, abscess, eclampsia, Creutzfeldt-Jakob disease, lupus
cerebritis, or invasive central nervous system procedures, e.g.,
neurosurgery, endovascular clot removal, spinal tap, aneurysm
repair, or deep brain stimulation or, e.g., spinal cord edema
consequent to spinal cord trauma, e.g., spinal cord compression; or
[0017] cerebral edema consequent to microgravity and/or radiation
exposure and/or optical nerve edema, e.g., optical nerve edema
consequent to microgravity and/or radiation exposure; or [0018]
retinal edema; or [0019] pulmonary edema; or [0020] hyponatremia or
excessive fluid retention, e.g., consequent to heart failure (HF),
liver cirrhosis, nephrotic disorder, syndrome of inappropriate
antidiuretic hormone secretion (SIADH), or infertility treatment;
or [0021] ovarian hyperstimulation syndrome; or [0022] epilepsy,
retinal ischemia or other diseases of the eye associated with
abnormalities in intraocular pressure and/or tissue hydration,
myocardial ischemia, myocardial ischemia/reperfusion injury,
myocardial infarction, myocardial hypoxia, congestive heart
failure, sepsis, neuromyelitis optica, or glioblastoma; or [0023]
fibromyalgia; or [0024] multiple sclerosis; or [0025] migraines,
comprising administering to a patient in need thereof an effective
amount of an aquaporin inhibitor, e.g., an inhibitor of AQP2 or
AQP4, for example a phenylbenzamide, e.g., niclosamide or a
compound of formula (I) as described in US 2010/0274051 A1 or U.S.
Pat. No. 7,700,655, e.g., a compound of general formulae (I),
(I-1), (I-2), (I-3), and (I-4) as set forth therein, e.g., selected
from Compound Nos. 1-223 as set forth in US 2010/0274051 or
Compound Nos. 301-555 as set forth in U.S. Pat. No. 7,700,655, or a
compound of formula (I) as described in U.S. Pat. No. 7,626,042,
e.g., selected from Compound Nos. 1-151 as set forth therein; for
example a compound of formula 1a:
[0025] ##STR00001## [0026] wherein R.sub.1, R.sub.2, R.sub.3,
R.sub.4, and R.sub.5 are selected from H, halo, halogenated
C.sub.1-4 alkyl (e.g., trifluoromethyl), and cyano; and R.sub.6 is
selected from H and physiologically hydrolysable and acceptable
acyl groups, [0027] in free or pharmaceutically acceptable salt
form.
[0028] The invention further provides high throughput assays for
identification of specific aquaporins, comprising measuring the
response of an aquaporin-expressing cell population versus a
control cell population to a hypertonic or hypotonic solution in
the presence or absence of a test compound.
[0029] The invention further provides a compound of formula
##STR00002##
[0030] Further areas of applicability of the present invention will
become apparent from the detailed description provided hereinafter.
It should be understood that the detailed description and specific
examples, while indicating the preferred embodiment of the
invention, are intended for purposes of illustration only and are
not intended to limit the scope of the invention.
BRIEF DESCRIPTION OF THE DRAWINGS
[0031] The present invention will become more fully understood from
the detailed description and the accompanying drawings,
wherein:
[0032] FIG. 1 depicts results of aquaporin-4 (FIG. 1A) and
aquaporin-2 (FIG. 1B) mediated cell volume change assay, and the
inhibitory effect of Compound 3 (compound of formula 1a where
R.sub.1, R.sub.3 and R.sub.5 are each chloro, and R.sub.2, R.sub.4
and R.sub.6 are H) against these aquaporins.
[0033] FIG. 2 depicts specificity of Compound 3 towards AQP-1,
AQP-2, AQP-4-M1, AQP-4-M23, and AQP-5.
[0034] FIG. 3 depicts a Hummel-Dryer style assay for [3H]-labeled
Compound 4 (compound of formula 1a where R.sub.1, R.sub.3 and
R.sub.5 are each trifluoromethyl, and R.sub.2, R.sub.4 and R.sub.6
are H) binding to purified AQP4b.
[0035] FIG. 4 depicts percent survival curves for the water
toxicity mouse model using 0.76 mg/kg Compound 1 (compound of
formula 1a where R.sub.1 is chloro, R.sub.3 and R.sub.5 are each
trifluoromethyl, and R.sub.2, R.sub.4 and R.sub.6 are H).
[0036] FIG. 5 depicts inhibition of cerebral edema formation by
Compound 1 in the mouse water toxicity model by MRI brain volume
analysis, with n=14 mice/treatment. A time course of edema
formation is shown comparing no drug vs. Compound 1 at 0.76 mg/kg.
The first time point at 5.67 min coincides with the scan slice at
the middle of the brain during the first post-injection scan. Other
time points are placed in a similar manner. The data is fitted to a
single exponential equation:
V/V.sub.0=+dV.sub.max(1-e(1-e.sup.(k-kt)); [0037] where
V/V.sub.0=relative brain volume, V.sub.i=initial relative brain
volume, dV.sub.max=maximum change in relative brain volume, k=first
order rate constant (min.sup.-1), and t=time in minutes.
[0038] FIG. 6 depicts the calcein fluorescence end-point assay used
for high throughput screening.
[0039] FIG. 7 depicts hit validation using the Cell Bursting
Aquaporin Assay; inset shows the structure of Compound 3.
[0040] FIG. 8 depicts reduction in intracranial pressure (ICP) in
the mouse water toxicity model with Compound 1 at 0.76 mg/kg.
[0041] FIG. 9 depicts plasma and serum levels of Compound 1
converted from
2-((3,5-bis(trifluoromethyl)phenyl)carbamoyl)-4-chlorophenyl
dihydrogen phosphate bis ethanolamine salt (shown below).
##STR00003##
[0042] FIG. 10 depicts mouse middle cerebral artery occlusion
(MCAo) model of ischemic stroke.
[0043] FIG. 11 depicts relative change in hemispheric brain volume
in the mouse middle cerebral artery occlusion (MCAo) model.
[0044] FIG. 12 depicts neurological outcome following MCAo in mice
treated with saline (no drug, ) or Compound 5 (.smallcircle.).
DETAILED DESCRIPTION OF THE INVENTION
[0045] The following description of the preferred embodiments is
merely exemplary in nature and is in no way intended to limit the
invention, its application, or uses.
[0046] Expression of Aquaporin-4 (AQP4) is upregulated in animal
models of trauma, stroke and water intoxication as well as around
human malignant brain tumors. Aquaporin-4 (AQP4) has been shown to
play a critical role in the development of cerebral and spinal cord
edema. AQP4 provides the primary route for water movement across
the BBB and glia limitans. AQP4 knockout mice, without the APQ4
gene, have improved survival compared to wild-type mice in models
of ischemic stroke, water toxicity, bacterial meningitis, and
spinal cord compression.
[0047] Cerebral edema (CE) is generally divided into 2 major
categories: vasogenic and cytotoxic. Vasogenic cerebral edema may
occur when a breach in the blood-brain barrier (BBB) allows water
and solutes to diffuse into the brain. It has been reported that
AQP4-null mice have increased brain edema in a model of
subarachnoid hemorrhage, suggesting that AQP4 may be required for
the clearance of water collected in intercellular space. In
contrast, cytotoxic cerebral edema may be initiated by ischemia
which results in reduced plasma osmolality rather than a disrupted
BBB. Ischemia may to a drop in ATP levels which is thought to slow
the Na--K ATPase pump resulting in an uptake of Na.sup.+ and
Cl.sup.- through leakage pathways. The net effect may be a cellular
osmotic imbalance, drawing H.sub.2O into cells--astrocytes more so
than neurons--and leading to increased ICP. Mouse models for
ischemic stroke, water toxicity, bacterial meningitis, and
spinal-cord compression fall into this category. In these models,
AQP4-null mice have reduced CE pointing to AQP4 as the central
pathway for water movement into the brain during the formation of
cytotoxic CE. However, cytotoxic and vasogenic edema are not
sharply divided categories; an injury that initially causes
cytotoxic edema may be followed later, e.g., within the next hours
to days, by vasogenic edema. This may suggest different treatments
for cerebral edema at different times.
[0048] Glioblastoma is a common and aggressive malignant primary
brain tumor Inhibition of AQP4 in U87 human gliobastoma cell lines
induces apoptosis.
[0049] It has been reported that propensity to epileptic seizures
is related to relative cellular and extracellular space (ECS)
volume. Hyperexcitability and increased epileptiform activity
results from hypotonic exposure which decreases ECS volume, while
attenuated epileptiform activity results from hyperosmolar medium.
Furosemide, which blocks seizure-induced cell swelling, has been
reported to inhibit epileptiform activity in vitro and in vivo.
AQP4 knockout mice were reported to have lower seizure
susceptibility to the convulsant pentylenetetrazol and a greater
electrographic seizure threshold when seizures were induced by
electrical stimulation in the hippocampus. It was also reported
that AQP4 knockout mice had more prolonged hippocampal-stimulation
evoked seizures compared to wild type mice.
[0050] AQP4 is expressed in the Muller cells in the retina. Studies
have implicated Muller cells in the pathogenesis of retinal injury
after ischemia. It has been reported that AQP4 deletion in mice
conferred significant preservation of retinal function and
architecture after retinal ischemia.
[0051] AQP4 is reportedly found in mammalian hearts. It has been
reported that AQP4 expression in the human heart is present at both
the mRNA and protein level. Water accumulates in the myocardium as
a result of ischemia, when ischemic tissue becomes hyperosmolar and
attracts water from the capillary lumen. The water is transported
into the myocardial cells, for example, into cardiomyocytes.
Reperfusion delivers normoosmolar blood to the hyperosmolar cells,
which leads to further cell swelling, which may even involve cells
outside the risk area. This water accumulation leads to a
pronounced depression of cardiac function, and aggravates effects
of shortage in oxygen and nutrient supply. Myocardial
ischemia/reperfusion injury refers to damage caused by ischemia
followed by reperfusion in the heart. It has been reported that
AQP4 knockout mice had reduced infarct size after both ex vivo
ischemia-reperfusion and after in vivo ischemia without
reperfusion. It was concluded that the AQP4 knockout genotype
conferred increased tolerance to ischemic injury.
[0052] Neuromyelitis optica (NMO) is a neuroinflammatory
demyelinating disease that primarily affects optic nerve and spinal
cord. A feature of NMO is the presence of serum antibodies directed
against extracellular epitopes on AQP4. It has been reported that
most, if not all, NMO patients are seropositive for AQP4
autoantibodies (NMO-IgG). It is thought that NMO-IgG binding to
AQP4 in astrocytes initiates an inflammatory cascade and the
consequent neuroinflammation and myelin loss produce neurological
deficits. Blocking binding of those antibodies to AQP4 could
prevent the initiation of the inflammatory cascade.
[0053] In one embodiment, the invention provides methods of
treating edema mediated by aquaporin, e.g., AQP4, wherein the edema
is consequent to hypoxia, e.g., general systemic hypoxia, e.g.,
hypoxia caused by an interruption of blood perfusion, for example
wherein the edema is cerebral edema consequent to hypoxia caused by
cardiac arrest, stroke, or other interruption of blood perfusion to
the brain, or wherein the edema is cardiac edema consequent to
cardiac ischemia or other interruption of blood flow to the heart.
Hypoxia can lead to development of metabolic acidosis (e.g. lactic
acidosis), which in turn leads to edema, and the edema itself can
then reduce blood perfusion, leading to cell death and poorer
outcomes, particularly in tissues where swelling is physically
constrained, for example within the skull or within the
pericardium. This hypoxia is believed to be why, for example,
patients who have been rescued from cardiac arrest may subsequently
exhibit brain swelling, as well as damage to the cardiac tissue.
Blocking aquaporin channels, e.g., AQP4, e.g., by administering an
aquaporin-inhibiting compound as described herein, inhibits or
controls this edema, thereby limiting further damage to the
affected tissue.
[0054] Aquaporin-2 (AQP2) is the primary route of water movement at
the collecting duct in the kidney. Blocking this water channel
would lower water reabsorption without incurring electrolyte
imbalances or interfering with vasopressin receptor-mediated
signaling. Evidence that an AQP2 blocker would not produce
electrolyte imbalances, and instead be an effective treatment for
hyponatremia, comes from patients with diabetes insipidus who lack
functional AQP2. They exhibit chronic aquaresis but--if normal
hydration is maintained--do not demonstrate any other consequence
of their long term loss of AQP2 function.
[0055] The invention thus provides the use of aquaporin inhibitors
in controlling diseases or conditions of water imbalance, including
edema, particularly edema of the brain and spinal cord, e.g.,
following trauma or ischemic stroke, as well as the edema
associated with glioma, meningitis, acute mountain sickness,
epileptic seizures, infections, metabolic disorders, hypoxia, water
intoxication, hepatic failure, hepatic encephalopathy, hypoxia, and
diabetic ketoacidosis by inhibiting water uptake through the BBB,
and also useful in treating and controlling hyponatremia and
excessive fluid retention, by inhibiting water uptake at the
kidneys. This invention also provides the use of aquaporin
inhibitors in controlling diseases or conditions including
epilepsy, retinal ischemia and other diseases of the eye associated
with abnormalities in intraocular pressure and/or tissue hydration,
myocardial ischemia, myocardial ischemia/reperfusion injury,
myocardial infarction, myocardial hypoxia, congestive heart
failure, sepsis, neuromyelitis optica, and migraines.
[0056] In one embodiment, the invention provides a method (Method
1) of treating or controlling a disease or condition mediated by an
aquaporin comprising administering to a patient in need thereof an
effective amount of a phenylbenzamide compound, e.g., an effective
amount of niclosamide
(5-chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide) or a
compound of Formula I:
##STR00004##
wherein X represents a connecting group whose number of atoms in
the main chain is 2 to 5 (said connecting group may be
substituted), A represents a hydrogen atom or an acyl group which
may be substituted, or a C.sub.1 to C.sub.6 alkyl group which may
be substituted, or A may bind to connecting group X to form a
cyclic structure which may be substituted, E represents an aryl
group which may be substituted or a heteroaryl group which may be
substituted, ring Z represents an arene which may have one or more
substituents in addition to the group represented by formula --O-A
wherein A has the same meaning as that defined above and the group
represented by formula --X-E wherein each of X and E has the same
meaning as that defined above, or a heteroarene which may have one
or more substituents in addition to the group represented by
formula --O-A wherein A has the same meaning as that defined above
and the group represented by formula --X-E wherein each of X and E
has the same meaning as that defined above; in free or
pharmaceutically acceptable salt form, including solvate or hydrate
forms; e.g. [0057] 1.1. Method 1 wherein the compound of Formula I
is selected from the compounds of formula (I) as described in US
2010/0274051 A1 or U.S. Pat. No. 7,700,655, e.g., a compound of
general formulas (I), (I-1), (I-2), (I-3), and (I-4) as set forth
therein, e.g., selected from Compound Nos. 1-223 as set forth in US
2010/0274051 or Compound Nos. 301-555 as set forth in U.S. Pat. No.
7,700,655. [0058] 1.2. Method 1.1 wherein the compound of Formula I
is selected from the free or pharmaceutically acceptable salt forms
of: [0059]
N-[3,5-bis(trifluoromethyl)phenyl]-5-fluoro-2-hydroxybenzamide,
[0060]
N-[3,5-bis(trifluoromethyl)phenyl]-5-cyano-2-hydroxybenzamide,
[0061]
N-[3,5-bis(trifluoromethyl)phenyl]-2-hydroxy-5-(trifluoromethyl)be-
nzamide, [0062]
N-[3,5-bis(trifluoromethyl)phenyl]-2-hydroxy-5-(1,1,2,2,2-pentafluoroethy-
l)benzamide, [0063]
N-[3,5-bis(trifluoromethyl)phenyl]-5-(2,2-dicyanoethen-1-yl)-2-hydroxyben-
zamide, [0064]
N-[3,5-bis(trifluoromethyl)phenyl]-5-ethynyl-2-hydroxybenzamide,
[0065]
N-[3,5-bis(trifluoromethyl)phenyl]-2-hydroxy-5-(phenylethynyl)benzamide,
[0066]
N-[3,5-bis(trifluoromethyl)phenyl]-2-hydroxy-5-[(trimethylsilyl)et-
hynyl]benzamide, [0067]
N-[3,5-bis(trifluoromethyl)phenyl]-4-hydroxybiphenyl-3-carboxamide,
[0068]
N-[3,5-bis(trifluoromethyl)phenyl]-2-hydroxy-5-(3-thienyl)benzamid-
e, [0069]
N-[3,5-bis(trifluoromethyl)phenyl]-2-hydroxy-5-(1-pyrrolyl)benza-
mide, [0070]
N-[3,5-bis(trifluoromethyl)phenyl]-2-hydroxy-5-(2-methylthiazol-4-yl)benz-
amide, [0071]
N-[3,5-bis(trifluoromethyl)phenyl]-2-hydroxy-5-(2-pyridyl)benzamide,
[0072]
N-[3,5-bis(trifluoromethyl)phenyl]-5-dimethylsulfamoyl-2-hydroxybe-
nzamide, [0073]
N-[3,5-bis(trifluoromethyl)phenyl]-2-hydroxy-5-(pyrrole-1-sulfonyl)benzam-
ide, [0074]
N-[2,5-bis(trifluoromethyl)phenyl]-5-chloro-2-hydroxybenzamide,
[0075]
N-(2,5-bis(trifluoromethyl)phenyl-5-bromo-2-hydroxybenzamide,
[0076]
2-acetoxy-N-[2,5-bis(trifluoromethyl)phenyl]-5-chlorobenzamide,
[0077]
2-acetoxy-N-[3,5-bis(trifluoromethyl)phenyl]-5-chlorobenzamide,
[0078]
5-chloro-N-[2-fluoro-3-(trifluoromethyl)phenyl]-2-hydroxybenzamide,
[0079]
5-chloro-N-[2-fluoro-5-(trifluoromethyl)phenyl]-2-hydroxybenzamide-
, [0080]
5-chloro-N-[2-chloro-5-(trifluoromethyl)phenyl]-2-hydroxybenzamid-
e, [0081]
5-bromo-N-[2-chloro-5-(trifluoromethyl)phenyl]-2-hydroxybenzamid-
e, [0082]
2-acetoxy-5-chloro-N-[2-chloro-5-(trifluoromethyl)phenyl]benzami-
de, [0083]
5-chloro-N-[3-fluoro-5-(trifluoromethyl)phenyl]-2-hydroxybenzam-
ide, [0084]
5-bromo-N-[3-bromo-5-(trifluoromethyl)phenyl]-2-hydroxybenzamide,
[0085]
5-chloro-N-[3-fluoro-5-(trifluoromethyl)phenyl]-2-hydroxybenzamide,
[0086]
5-chloro-N-[4-fluoro-3-(trifluoromethyl)phenyl]-2-hydroxybenzamide-
, [0087]
5-bromo-N-[4-chloro-3-(trifluoromethyl)phenyl]-2-hydroxybenzamide-
, [0088]
5-chloro-2-hydroxy-N-[2-nitro-5-(trifluoromethyl)phenyl]benzamide-
, [0089]
5-bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxybenzamide,
[0090]
5-chloro-2-hydroxy-N-[2-methyl-3-(trifluoromethyl)phenyl]benzamide-
, [0091]
5-chloro-2-hydroxy-N-[2-methyl-5-(trifluoromethyl)phenyl]benzamid-
e, [0092]
2-hydroxy-5-methyl-N-[2-methyl-5-(trifluoromethyl)phenyl]benzami-
de, [0093]
5-chloro-2-hydroxy-N-[4-methyl-3-(trifluoromethyl)phenyl]benzam-
ide, [0094]
2-hydroxy-5-methyl-N-[4-methyl-3-(trifluoromethyl)phenyl]benzamide,
[0095]
5-bromo-2-hydroxy-N-[2-methoxy-5-(trifluoromethyl)phenyl]benzamide-
, [0096]
5-chloro-2-hydroxy-N-[2-methoxy-5-trifluoromethyl)phenyl]benzamid-
e, [0097]
5-bromo-2-hydroxy-N-[3-methoxy-5-(trifluoromethyl)phenyl]benzami-
de, [0098]
5-chloro-2-hydroxy-N-[4-methoxy-3-(trifluoromethyl)phenyl]benza-
mide, [0099]
5-chloro-2-hydroxy-N-[2-methylsulfanyl-5-(trifluoromethyl)phenyl]benzamid-
e, [0100]
5-chloro-2-hydroxy-N-[2-(1-pyrrolidino)-5-(trifluoromethyl)pheny-
l]benzamide, [0101]
5-chloro-2-hydroxy-N-[2''-morpholino-5-(trifluoromethyl)phenyl]benzamide,
[0102]
5-bromo-N-[5-bromo-4-(trifluoromethyl)thiazol-2-yl]-2-hydroxybenza-
mide, [0103]
5-chloro-N-{5-cyano-4-[(1,1-dimethyl)ethyl]thiazol-2-yl}-2-hydroxybenzami-
de, [0104]
5-bromo-N-{5-cyano-4-[(1,1-dimethyl)ethyl]thiazol-2-yl}-2-hydro-
xybenzamide, [0105] 2-(5-bromo-2-hydroxybenzoyl)amino-4
(trifluoromethyl)thiazol-5-carboxylic acid ethylester. [0106] 1.3.
Method 1 wherein A is C.sub.1-4 acyl (e.g. acetyl). [0107] 1.4.
Method 1 wherein the compound is a compound of formula I as
described in U.S. Pat. No. 7,626,042, for example of formula I-1,
e.g. any of Compound Nos. 1-151 as described in U.S. Pat. No.
7,626,042. [0108] 1.5. Method 1.4 wherein A is C.sub.1-4 acyl (e.g.
acetyl). [0109] 1.6. Method 1 wherein A is the residue of an amino
acid. [0110] 1.7. Method 1 wherein A is a 5 to 6-membered
non-aromatic heterocyclic ring-carbonyl group, for example a 5 to
6-membered non-aromatic heterocyclic ring-carbonyl group which
comprises at least one nitrogen atom as ring-constituting atoms
(ring forming atoms) of said heterocyclic ring and binds to the
carbonyl group at the nitrogen atom, e.g., wherein said 5 to
6-membered non-aromatic heterocyclic ring is selected from
1-pyrrolidinyl group, piperidino group, morpholino group, and
1-piperazinyl group, and said heterocyclic ring may be substituted
with one or more substituents, e.g., independently selected from an
alkyl group, an alkyl-oxy-carbonyl group, and a carboxy group; for
example wherein A is (morpholin-4-yl)carbonyl. [0111] 1.8. Method 1
wherein A is a N,N-di-substituted carbamoyl group, wherein two
substituents of said carbamoyl group may combine to each other,
together with the nitrogen atom to which they bind, to form a
nitrogen-containing heterocyclic group which may be substituted.
[0112] 1.9. Method 1 wherein A is (morpholin-4-yl)carbonyl. [0113]
1.10. Method 1 wherein A is a phosphono group, which may be
substituted, e.g., dibenzyl phosphono, or unsubstituted. [0114]
1.11. Method 1 wherein the compound of Formula I is a compound of
formula 1a:
[0114] ##STR00005## [0115] wherein R.sub.1, R.sub.2, R.sub.3,
R.sub.4, and R.sub.5 are selected from H, halo, halogenated
C.sub.1-4 alkyl (e.g., trifluoromethyl), and cyano; and R.sub.6 is
selected from H and physiologically hydrolysable and acceptable
acyl, e.g., wherein R.sub.6 is A as hereinbefore defined in any of
Methods 1-1.9; [0116] in free, pharmaceutically acceptable salt
form. [0117] 1.12. Method 1.11 wherein the compound of Formula I is
a compound of formula 1a wherein R.sub.1 is selected from
trifluoromethyl, chloro, fluoro, and bromo; R.sub.3 and R.sub.5 are
the same or different and selected from trifluoromethyl, chloro,
fluoro, and bromo; and R.sub.2 and R.sub.4 are both H. [0118] 1.13.
Method 1.12 wherein the compound of Formula I is a compound of
formula 1a wherein R.sub.1 is selected from chloro and bromo;
R.sub.3 and R.sub.5 are both trifluoromethyl; and R.sub.2, R.sub.4
and R.sub.6 are all H, e.g., wherein the compound of formula 1a is
selected from:
[0118] ##STR00006## [0119] 1.14. Method 1.11 or 1.12 wherein
R.sub.6 is H. [0120] 1.15. Method 1.11 or 1.12 wherein R.sub.6 is
acetyl. [0121] 1.16. Method 1.11 or 1.12 wherein the compound of
Formula I is a compound of formula 1a wherein R.sub.1 is selected
from chloro and bromo; R.sub.3 and R.sub.5 are both
trifluoromethyl; and R.sub.2 and R.sub.4 are H and R.sub.6 is
acetyl, e.g., wherein the compound of formula 1a is selected
from:
[0121] ##STR00007## [0122] 1.17. Method 1.13 wherein the compound
of formula 1a is Compound 1
[0122] ##STR00008## [0123] 1.18. Method 1.12 wherein the compound
of Formula I is a compound of formula 1a wherein R.sub.1, R.sub.3
and R.sub.5 are each chloro, and R.sub.2, R.sub.4 and R.sub.6 are
each H (Compound 3). [0124] 1.19. Method 1.12 wherein the compound
of Formula I is a compound of formula 1a wherein R.sub.1, R.sub.3
and R.sub.5 are each trifluoromethyl, and R.sub.2, R.sub.4 and
R.sub.6 are each H (Compound 4). [0125] 1.20. Method 1.11 or 1.12
wherein the compound of Formula I is a compound of formula 1a, and
R.sub.6 is C.sub.1-4 acyl (e.g. acetyl). [0126] 1.21. Method 1.11
or 1.12 wherein the compound of Formula I is a compound of formula
1a, and R.sub.6 is the residue of an amino acid. [0127] 1.22.
Method 1.11 or 1.12 wherein the compound of Formula I is a compound
of formula 1a, and R.sub.6 is a 5 to 6-membered non-aromatic
heterocyclic ring-carbonyl group, for example a 5 to 6-membered
non-aromatic heterocyclic ring-carbonyl group which comprises at
least one nitrogen atom as ring-constituting atoms (ring forming
atoms) of said heterocyclic ring and binds to the carbonyl group at
the nitrogen atom, e.g., wherein said 5 to 6-membered non-aromatic
heterocyclic ring is selected from 1-pyrrolidinyl group, piperidino
group, morpholino group, and 1-piperazinyl group, and said
heterocyclic ring may be substituted with one or more substituents,
e.g., independently selected from an alkyl group, an
alkyl-oxy-carbonyl group, and a carboxy group; for example wherein
R.sub.6 is (morpholin-4-yl)carbonyl. [0128] 1.23. Method 1.11 or
1.12 wherein the compound of Formula I is a compound of formula 1a,
and R.sub.6 is a N,N-di-substituted carbamoyl group, wherein two
substituents of said carbamoyl group may combine to each other,
together with the nitrogen atom to which they bind, to form a
nitrogen-containing heterocyclic group which may be substituted.
[0129] 1.24. Method 1.11 or 1.12 wherein the compound of Formula I
is a compound of formula 1a, and R.sub.6 is a
(morpholin-4-yl)carbonyl group. [0130] 1.25. Method 1.11 or 1.12
wherein the compound of Formula I is a compound of formula 1a, and
R.sub.6 is a phosphono group, which may be substituted, e.g.
dibenzylphosphono, or unsubstituted. [0131] 1.26. Method 1.25
wherein the compound of formula 1a is selected from:
[0131] ##STR00009## [0132] 1.27. Method 1.26 wherein the compound
of formula 1a is Compound 5
[0132] ##STR00010## [0133] 1.28. Method 1 wherein the
phenylbenzamide compound is niclosamide or the compound shown
below
[0133] ##STR00011## [0134] 1.29. Any of Method 1, et seq. wherein
the aquaporin is AQP4. [0135] 1.30. Any of Method 1, et seq.
wherein the condition to be treated or controlled is selected from
edema, e.g. edema of the brain or spinal cord, e.g., cerebral
edema, e.g. cerebral edema consequent to head trauma, ischemic
stroke, glioma, meningitis, acute mountain sickness, epileptic
seizures, infections, metabolic disorders, water intoxication,
hepatic failure, hepatic encephalopathy, or diabetic ketoacidosis
or, e.g., spinal cord edema, e.g., spinal cord edema consequent to
spinal cord trauma, e.g., spinal cord compression. [0136] 1.31.
Method 1.30 further comprising a treatment selected from one or
more of the following: optimal head and neck positioning to
facilitate venous outflow, e.g. head elevation 30.degree.;
avoidance of dehydration; systemic hypotension; maintenance of
normothermia or hypothermia; aggressive measures; osmotherapy,
e.g., using mannitol or hypertonic saline; hyperventilation;
therapeutic pressor therapy to enhance cerebral perfusion;
administration of barbiturates to reduce cerebral metabolism
(CMO.sub.2); hemicraniectomy; administration of aspirin;
administration of amantadine; intravenous thrombolysis (e.g. using
rtPA); mechanical clot removal; angioplasty; and/or stents. [0137]
1.32. Any of Method 1, et seq. wherein the patient is at elevated
risk of cerebral edema, e.g., due to head trauma, ischemic stroke,
glioma, meningitis, acute mountain sickness, epileptic seizure,
infection, metabolic disorder, water intoxication, hepatic failure,
hepatic encephalopathy, or diabetic ketoacidosis. [0138] 1.33.
Method 1.30 wherein the patient has suffered a stroke, head injury,
or spinal injury. [0139] 1.34. Method 1.33 wherein the patient has
suffered a stroke, head injury or spinal injury within 12 hours,
e.g. within 6 hours, preferably within 3 hours of commencing
treatment. [0140] 1.35. Method 1.30 wherein the patient is at
elevated risk of suffering a stroke, head injury or spinal injury,
e.g., in combat or in an athletic competition. [0141] 1.36. Any of
Method 1, et seq. wherein the patient already has cerebral edema.
[0142] 1.37. Any of Method 1, et seq. wherein the condition to be
treated or controlled is cerebral edema consequent to a stroke or a
traumatic brain injury. [0143] 1.38. Any of Method 1, et seq.
wherein the condition to be treated or controlled is cerebral edema
consequent to a middle cerebral artery stroke. [0144] 1.39. Any of
Method 1, et seq. wherein the condition to be treated or controlled
is cerebral edema consequent to closed head trauma. [0145] 1.40.
Any of Methods 1-1.32 wherein the condition to be treated or
controlled is cerebral edema consequent to an epileptic seizure.
[0146] 1.41. Any of Methods 1-1.32 wherein the condition to be
treated or controlled is cerebral edema consequent to an infection.
[0147] 1.42. Any of Methods 1-1.32 wherein the condition to be
treated or controlled is cerebral edema consequent to a metabolic
disorder. [0148] 1.43. Any of Methods 1-1.32 wherein the condition
to be treated or controlled is cerebral edema consequent to glioma.
[0149] 1.44. Any of Methods 1-1.32 wherein the condition to be
treated or controlled is cerebral edema consequent to meningitis,
acute mountain sickness, or water intoxication. [0150] 1.45. Any of
Methods 1-1.32 wherein the condition to be treated or controlled is
cerebral edema consequent to hepatic failure, hepatic
encephalopathy, or diabetic ketoacidosis. [0151] 1.46. Any of
Methods 1-1.31 wherein the condition to be treated or controlled is
cerebral edema consequent to an abscess. [0152] 1.47. Any of
Methods 1-1.31 wherein the condition to be treated or controlled is
cerebral edema consequent to eclampsia. [0153] 1.48. Any of Methods
1-1.31 wherein the condition to be treated or controlled is
cerebral edema consequent to Creutzfeldt-Jakob disease. [0154]
1.49. Any of Methods 1-1.31 wherein the condition to be treated or
controlled is cerebral edema consequent to lupus cerebritis. [0155]
1.50. Any of Methods 1-1.31 wherein the condition to be treated or
controlled is edema consequent to hypoxia, e.g., general systemic
hypoxia, e.g., hypoxia caused by an interruption of blood
perfusion, for example wherein the edema is cerebral edema
consequent to hypoxia caused by cardiac arrest, stroke, or other
interruption of blood perfusion to the brain, or wherein the edema
is cardiac edema consequent to cardiac ischemia or other
interruption of blood flow to the heart. [0156] 1.51. Any of
Methods 1-1.31 wherein the condition to be treated or controlled is
cerebral consequent to microgravity and/or radiation exposure,
e.g., exposure from space flight or from working with radioactive
materials or from working in radioactive areas and/or optic nerve
edema, e.g., optic nerve edema consequent to microgravity and/or
radiation exposure, e.g., exposure from space flight or from
working with radioactive materials or from working in radioactive
areas. [0157] 1.52. Any of Methods 1-1.31 wherein the condition to
be treated or controlled is cerebral edema consequent to an
invasive central nervous system procedures, e.g., neurosurgery,
endovascular clot removal, spinal tap, aneurysm repair, or deep
brain stimulation. [0158] 1.53. Method 1.51 or 1.52 wherein the
patient is at elevated risk of edema, e.g., due to microgravity
and/or radiation exposure, neurosurgery, endovascular clot removal,
spinal tap, aneurysm repair, or deep brain stimulation. [0159]
1.54. Method 1.51 or 1.52 wherein the patient already has edema.
[0160] 1.55. Any of Methods 1, et seq. wherein the edema is
cytotoxic cerebral edema or is primarily cytotoxic cerebral edema.
[0161] 1.56. Any of Methods 1-1.45 or 1.50 wherein the edema is
cytotoxic cerebral edema or is primarily cytotoxic cerebral edema.
[0162] 1.57. Any of Methods 1-1.30 wherein the condition to be
treated or controlled is spinal cord edema, e.g., spinal cord edema
consequent to a spinal cord trauma, e.g., spinal cord compression.
[0163] 1.58. Method 1.57 wherein the condition to be treated or
controlled is spinal cord edema consequent to spinal cord
compression. [0164] 1.59. Any of Methods 1-1.30 wherein the
condition to be treated or controlled is retinal edema. [0165]
1.60. Any of Methods 1-1.30 wherein the condition to be treated or
controlled is pulmonary edema. [0166] 1.61. Any of Methods 1-1.29
wherein the condition to be treated or controlled is epilepsy.
[0167] 1.62. Any of Methods 1-1.29 wherein the condition to be
treated or controlled is retinal ischemia or other diseases of the
eye associated with abnormalities in intraocular pressure and/or
tissue hydration. [0168] 1.63. Any of Methods 1-1.29 wherein the
condition to be treated or controlled is myocardial ischemia.
[0169] 1.64. Any of Methods 1-1.29 wherein the condition to be
treated or controlled is myocardial ischemia/reperfusion injury.
[0170] 1.65. Any of Methods 1-1.29 wherein the condition to be
treated or controlled is myocardial infarction. [0171] 1.66. Any of
Methods 1-1.29 wherein the condition to be treated or controlled is
myocardial hypoxia. [0172] 1.67. Any of Methods 1-1.29 wherein the
condition to be treated or controlled is congestive heart failure.
[0173] 1.68. Any of Methods 1-1.29 wherein the condition to be
treated or controlled is sepsis. [0174] 1.69. Any of Methods 1-1.29
wherein the condition to be treated or controlled is a migraine.
[0175] 1.70. Any of Methods 1-1.29 wherein the condition to be
treated or controlled is glioblastoma. [0176] 1.71. Any of Methods
1-1.29 wherein the condition to be treated or controlled is
fibromyalgia. [0177] 1.72. Any of Methods 1-1.29 wherein the
condition to be treated or controlled is multiple sclerosis. [0178]
1.73. Any of Methods 1-1.28 wherein the aquaporin is AQP2. [0179]
1.74. Any of Methods 1-1.28 or 1.73 wherein the condition to be
treated is hyponatremia or excessive fluid retention, e.g.,
consequent to heart failure (HF), for example congestive heart
failure, liver cirrhosis, nephrotic disorder, syndrome of
inappropriate antidiuretic hormone secretion (SIADH), or
infertility treatment, e.g., infertility treatment. [0180] 1.75.
Any of Methods 1-1.28 or 1.73 wherein the condition to be treated
or controlled is ovarian hyperstimulation syndrome. [0181] 1.76.
Any of Methods 1-1.28, 1.73, 1.74, or 1.75 further comprising one
or more of restriction of dietary sodium, fluid and/or alcohol;
and/or administration of one or more diuretics, vasopressin
receptor antagonists, angiotensin converting enzyme (ACE)
inhibitors, aldosterone inhibitors, angiotensin receptor blockers
(ARBs), beta-adrenergic antagonists (beta-blockers), and/or
digoxin. [0182] 1.77. Any of Method 1, et seq. wherein the
niclosamide or the compound of Formula I or formula 1a inhibits
aquaporin activity, e.g., AQP2 and/or AQP4 activity, by at least
50% at concentrations of 10 micromolar or less, for example
inhibits APQ2 and/or AQP4 activity by at least 50% at
concentrations of 10 micromolar or less in an aquaporin-mediated
cell volume change assay, e.g., is active in any of the assays of
Method 10, et seq. infra. [0183] 1.78. Any of Methods 1-1.29
wherein the condition to be treated or controlled is neuromyelitis
optica. [0184] 1.79. Any of Method 1, et seq. wherein the
niclosamide or the compound of Formula I or formula 1a is
administered orally. [0185] 1.80. Any of Method 1, et seq. wherein
the niclosamide or the compound of Formula I or formula 1a is
administered parenterally. [0186] 1.81. Method 1.80 wherein the
niclosamide or the compound of Formula I or formula 1a is
administered intravenously. [0187] 1.82. Any of Method 1, et seq.
wherein the patient is human. [0188] 1.83. Any of Method 1, et seq.
wherein the onset of action of any of the compounds identified in
Methods 1-1.28 is fairly rapid.
[0189] The invention further provides a phenylbenzamide, e.g.
niclosamide or a compound of Formula I or formula 1a as
hereinbefore described, for use in treating or controlling a
disease or condition mediated by an aquaporin, e.g., in any of
Methods 1, 1.1, et seq.
[0190] The invention further provides a phenylbenzamide, e.g.
niclosamide or a compound of Formula I or formula 1a as
hereinbefore described, in the manufacture of a medicament for
treating or controlling a disease or condition mediated by an
aquaporin, e.g., for use in any of Methods 1, 1.1, et seq.
[0191] The invention further provides a pharmaceutical composition
comprising a phenylbenzamide, e.g. niclosamide or a compound of
Formula I or formula 1a as hereinbefore described, in combination
with a pharmaceutically acceptable diluent or carrier for use in
treating or controlling a disease or condition mediated by an
aquaporin, e.g., in any of Methods 1, 1.1, et seq.
[0192] Phenylbenzamides, e.g. of Formula I or formula 1a as
hereinbefore described, may exist in free or salt form, e.g., as
acid addition salts. In this specification unless otherwise
indicated language such as "compound of Formula I or formula 1a" or
"compounds of Formula I or formula 1a" is to be understood as
embracing the compounds in any form, for example free base or acid
addition salt form. Pharmaceutically acceptable salts are known in
the art and include salts which are physiologically acceptable at
the dosage amount and form to be administered, for example
hydrochlorides.
[0193] Examples of the acyl group include, for example, formyl,
glyoxyloyl group, thioformyl group, carbamoyl group, thiocarbamoyl
group, sulfamoyl group, sulfinamoyl group, carboxy group, sulfo
group, phosphono group, and groups represented by the following
formulas:
##STR00012##
wherein R.sup.a1 and R.sup.b1 may be the same or different and
represent a hydrocarbon group or a heterocyclic group, or R.sup.a1
and R.sup.b1 combine to each other, together with the nitrogen atom
to which they bind, to form a cyclic amino group. Acyl includes
physiologically hydrolysable and acceptable acyl group. Examples of
the acyl group of "an acyl group which may be substituted" as used
herein, e.g., in relation to "A" include similar groups to the acyl
group in the aforementioned definition. "A" is a group selected
from the following substituent group .omega.: [Substitutent group
.omega.] a hydrocarbon-carbonyl group which may be substituted, a
heterocyclic ring-carbonyl group which may be substituted, a
hydrocarbon-oxy-carbonyl group which may be substituted, a
hydrocarbon-sulfonyl group which may be substituted, a sulfamoyl
group which may be substituted, a sulfo group which may be
substituted, a phosphono group which may be substituted, and a
carbamoyl group which may be substituted. By the term
"physiologically hydrolysable and acceptable acyl" as used herein,
e.g., in relation to "A" or "R.sub.6" in compounds of Formula I or
formula 1a, is meant a residue of an acid, for example a carboxylic
acid, a carbamic acid or a phosphoric acid (e.g., optionally
substituted carbonyl such as acetyl or the residue of an amino
acid, optionally substituted carbamoyl, e.g.
(morpholin-4-yl)carbonyl, or optionally substituted phosphono e.g.,
dibenzylphosphono), linked to an oxygen, e.g., as depicted in
Formula 1 or formula 1a above, e.g. to form an ester or
phosphoester with a compound of Formula I or formula 1a, which is
capable of hydrolysis from said oxygen under physiological
conditions to yield an acid which is physiologically tolerable at
doses to be administered, together with the corresponding hydroxy
compound of Formula I or formula 1a wherein A or R.sub.6 is H. As
will be appreciated the term thus embraces conventional
pharmaceutical prodrug forms, although it is not necessarily
required that the compounds must be hydrolyzed in order to be
active. The acyl compounds may be prepared by conventional means,
e.g., by acylation of a compound of Formula 1 or formula 1a,
wherein A or R.sub.6 is H, with the desired acid or acid halide.
Examples of acylated compounds and methods of making them are
provided, e.g., in US 2010/0274051 A1, U.S. Pat. No. 7,700,655, and
in U.S. Pat. No. 7,626,042, each incorporated herein by
reference.
[0194] The term "patient" includes human or non-human (i.e.,
animal) patient. In a particular embodiment, the invention
encompasses both human and nonhuman. In another embodiment, the
invention encompasses nonhuman. In another embodiment, the term
encompasses human.
[0195] The term "fairly rapid" with respect to onset of action
means that the time it takes after a compound is administered for a
response to be observed is 30 minutes or less, for example 20
minutes or less, for example or 15 minutes or less, for example 10
minutes or less, for example 5 minutes or less, for example 1
minute or less.
[0196] Phenylbenzamides, e.g. of Formula 1 or formula 1a as
hereinbefore described for use in the methods of the invention may
be used as a sole therapeutic agent, but may also be used in
combination or for co-administration with other active agents, for
example in conjunction with conventional therapies for cerebral
edema, stroke, traumatic brain injury, glioma, meningitis, acute
mountain sickness, infection, metabolic disorder, hypoxia, water
intoxication, hepatic failure, hepatic encephalopathy, diabetic
ketoacidosis, abscess, eclampsia, Creutzfeldt-Jakob disease, lupus
cerebritis, edema of the optic nerve, hyponatremia, fluid
retention, ovarian hyperstimulation syndrome, epilepsy, retinal
ischemia or other diseases of the eye associated with abnormalities
in intraocular pressure and/or tissue hydration, myocardial
ischemia, myocardial ischemia/reperfusion injury, myocardial
infarction, myocardial hypoxia, congestive heart failure, sepsis,
neuromyelitis optica, glioblastoma, or migraines.
[0197] In a further embodiment, the invention provides a method
(Method 2) of treating or controlling edema, e.g. edema of the
brain or spinal cord, e.g., cerebral edema, e.g. cerebral edema
consequent to head trauma, ischemic stroke, glioma, meningitis,
acute mountain sickness, epileptic seizures, infections, metabolic
disorders, hypoxia, water intoxication, hepatic failure, hepatic
encephalopathy, diabetic ketoacidosis, abscess, eclampsia,
Creutzfeldt-Jakob disease, or lupus cerebritis, as well as edema
consequent to microgravity and/or radiation exposure, as well as
edema consequent to invasive central nervous system procedures,
e.g., neurosurgery, endovascular clot removal, spinal tap, aneurysm
repair, or deep brain stimulation or, e.g., retinal edema or, e.g.,
spinal cord edema, e.g., spinal cord edema consequent to spinal
cord trauma, e.g., spinal cord compression, or e.g., pulmonary
edema, comprising administering an effective amount of an inhibitor
of AQP4, e.g, a compound binding to AQP4, to a patient in need
thereof, e.g., wherein the inhibitor of AQP4 is selected from
phenylbenzamides, e.g. niclosamide or a compound of Formula I or
formula 1a as hereinbefore described, e.g., any of the compounds
identified in Methods 1-1.28 above, for example [0198] 2. [0199]
2.1. Method 2 further comprising a treatment selected from one or
more of the following: optimal head and neck positioning to
facilitate venous outflow, e.g. head elevation 30.degree.;
avoidance of dehydration; systemic hypotension; maintenance of
normothermia or hypothermia; aggressive measures; osmotherapy,
e.g., using mannitol or hypertonic saline; hyperventilation;
therapeutic pressor therapy to enhance cerebral perfusion;
administration of barbiturates to reduce of cerebral metabolism
(CMO.sub.2); hemicraniectomy; administration of aspirin;
administration of amantadine; intravenous thrombolysis (e.g. using
rtPA); mechanical clot removal; angioplasty; and/or stents. [0200]
2.2. Method 2 or 2.1 wherein the patient is at elevated risk of
cerebral edema, e.g., due to head trauma, ischemic stroke, glioma,
meningitis, acute mountain sickness epileptic seizure, infection,
metabolic disorder, water intoxication, hepatic failure, hepatic
encephalopathy, or diabetic ketoacidosis. [0201] 2.3. Method 2,
2.1, or 2.2 wherein the patient has suffered a stroke, head injury,
or spinal injury. [0202] 2.4. Any of Method 2, et seq. wherein the
patient has suffered a stroke, head injury or spinal injury within
12 hours, e.g. within 6 hours, preferably within 3 hours of
commencing treatment. [0203] 2.5. Any of Method 2, et seq. wherein
the patient is at elevated risk of suffering a stroke, head injury
or spinal injury, e.g., in combat or in an athletic competition.
[0204] 2.6. Any of Method 2, et seq. wherein the patient already
has cerebral edema. [0205] 2.7. Any of Method 2, et seq. wherein
the condition to be treated or controlled is cerebral edema
consequent to a stroke or a traumatic brain injury. [0206] 2.8. Any
of Method 2, et seq. wherein the condition to be treated or
controlled is cerebral edema consequent to a middle cerebral artery
stroke. [0207] 2.9. Any of Method 2, et seq. wherein the condition
to be treated or controlled is cerebral edema consequent to a
closed head trauma. [0208] 2.10. Any of Methods 2-2.2 wherein the
condition to be treated or controlled is cerebral edema consequent
to an epileptic seizure. [0209] 2.11. Any of Methods 2-2.2 wherein
the condition to be treated or controlled is cerebral edema
consequent to an infection. [0210] 2.12. Any of Methods 2-2.2
wherein the condition to be treated or controlled is cerebral edema
consequent to a metabolic disorder. [0211] 2.13. Any of Methods
2-2.2 wherein the condition to be treated or controlled is cerebral
edema consequent to glioma. [0212] 2.14. Any of Methods 2-2.2
wherein the condition to be treated or controlled is cerebral edema
consequent to meningitis, acute mountain sickness, or water
intoxication. [0213] 2.15. Any of Methods 2-2.2 wherein the
condition to be treated or controlled is cerebral edema consequent
to hepatic failure, hepatic encephalopathy, or diabetic
ketoacidosis. [0214] 2.16. Method 2 or 2.1 wherein the condition to
be treated or controlled is cerebral edema consequent to an
abscess. [0215] 2.17. Method 2 or 2.1 wherein the condition to be
treated or controlled is cerebral edema consequent to eclampsia.
[0216] 2.18. Method 2 or 2.1 wherein the condition to be treated or
controlled is cerebral edema consequent to Creutzfeldt-Jakob
disease. [0217] 2.19. Method 2 or 2.1 wherein the condition to be
treated or controlled is cerebral edema consequent to lupus
cerebritis. [0218] 2.20. Method 2 or 2.1 wherein the condition to
be treated or controlled is cerebral consequent to microgravity
exposure, e.g., exposure from space flight or from working with
radioactive materials or from working in radioactive areas and/or
optic nerve edema, e.g., consequent to microgravity exposure, e.g.,
exposure from space flight or from working with radioactive
materials or from working in radioactive areas. [0219] 2.21. Method
2 or 2.1 wherein the condition to be treated or controlled is
cerebral edema consequent to invasive central nervous system
procedures, e.g., neurosurgery, endovascular clot removal, spinal
tap, aneurysm repair, or deep brain stimulation. [0220] 2.22.
Method 2.20 or 2.21 wherein the patient is at elevated risk of
edema, e.g., due to microgravity and/or radiation exposure,
neurosurgery, endovascular clot removal, spinal tap, aneurysm
repair, or deep brain stimulation. [0221] 2.23. Method 2.20 or 2.21
wherein the patient already has edema. [0222] 2.24. Any of Methods
2, et seq. wherein the edema is cytotoxic cerebral edema or is
primarily cytotoxic cerebral edema. [0223] 2.25. Any of Methods
2-2.15, et seq. wherein the edema is cytotoxic cerebral edema or is
primarily cytotoxic cerebral edema. [0224] 2.26. Method 2 wherein
the condition to be treated or controlled is spinal cord edema,
e.g., spinal cord edema consequent to spinal cord trauma, e.g.,
spinal cord compression. [0225] 2.27. Method 2.26 wherein the
condition to be treated or controlled is spinal cord edema
consequent to spinal cord compression. [0226] 2.28. Method 2
wherein the condition to be treated or controlled is retinal edema.
[0227] 2.29. Method 2 wherein the condition to be treated or
controlled is pulmonary edema. [0228] 2.30. Any of Method 2, et
seq. wherein the AQP4 inhibitor inhibits AQP4 activity by at least
50% at concentrations of 10 micromolar or less, for example
inhibits AQP4 activity by at least 50% at concentrations of 10
micromolar or less in an aquaporin-mediated cell volume change
assay, e.g., is active in any of the assays of Method 10, et seq.
infra. [0229] 2.31. Any of Method 2, et seq. wherein the duration
of treatment with an AQP4 inhibitor is less than 21 days, e.g.,
less than 2 weeks, e.g., one week or less. [0230] 2.32. Any of
Method 2, et seq. wherein the AQP4 inhibitor is administered
orally. [0231] 2.33. Any of Method 2, et seq. wherein the AQP4
inhibitor is administered parenterally. [0232] 2.34. Method 2.33
wherein the AQP4 inhibitor is administered intravenously. [0233]
2.35. Any of Method 2, et seq. wherein the patient is human. [0234]
2.36. Any of Method 2, et seq. wherein the onset of action of any
of the compounds identified in Methods 1-1.28 is fairly rapid.
[0235] 2.37. Any of Method 2, et seq. wherein the edema is
consequent to hypoxia, e.g., general systemic hypoxia, e.g.,
hypoxia caused by an interruption of blood perfusion, for example
wherein the edema is cerebral edema consequent to hypoxia caused by
cardiac arrest or other interruption of blood perfusion to the
brain.
[0236] In a further embodiment, the invention provides a method
(Method 3) of treating or controlling a condition selected from
hyponatremia and excessive fluid retention, e.g., consequent to
heart failure (HF), for example congestive heart failure, liver
cirrhosis, nephrotic disorder, syndrome of inappropriate
antidiuretic hormone secretion (SIADH), or infertility treatment,
e.g., infertility treatment, comprising administering an effective
amount of an inhibitor of AQP2, e.g., a compound binding to AQP2,
e.g., to a patient in need thereof, e.g., wherein the inhibitor of
AQP2 is selected from phenylbenzamides, e.g. niclosamide or a
compound of Formula I or formula 1a as hereinbefore described,
e.g., any of the compounds identified in Methods 1-1.28 above, for
example [0237] 3. [0238] 3.1. Method 3 wherein the condition to be
treated or controlled is ovarian hyperstimulation syndrome. [0239]
3.2. Method 3 or 3.1 further comprising one or more of restriction
of dietary sodium, fluid and/or alcohol; and/or administration of
one or more diuretics, vasopressin receptor antagonists,
angiotensin converting enzyme (ACE) inhibitors, aldosterone
inhibitors, angiotensin receptor blockers (ARBs), beta-adrenergic
antagonists (beta-blockers), and/or digoxin. [0240] 3.3. Any of
Method 3, et seq. wherein the AQP2 inhibitor inhibits AQP2 activity
by at least 50% at concentrations of 10 micromolar or less, for
example inhibits APQ2 activity by at least 50% at concentrations of
10 micromolar or less in an aquaporin-mediated cell volume change
assay, e.g., is active in any of the assays of Method 10, et seq.
infra. [0241] 3.4. Any of Method 3, et seq. wherein the AQP2
inhibitor is administered orally. [0242] 3.5. Any of Method 3, et
seq. wherein the AQP2 inhibitor is administered parenterally.
[0243] 3.6. Method 3.5 wherein the AQP2 inhibitor is administered
intravenously. [0244] 3.7. Any of Method 3, et seq. wherein the
patient is human. [0245] 3.8. Any of Method 3, et seq. wherein the
onset of action of any of the compounds identified in Methods
1-1.28 is fairly rapid.
[0246] In a further embodiment, the invention provides a method
(Method 4) of treating or controlling a condition selected from
epilepsy, retinal ischemia or other diseases of the eye associated
with abnormalities in intraocular pressure and/or tissue hydration,
myocardial ischemia, myocardial ischemia/reperfusion injury,
myocardial infarction, myocardial hypoxia, congestive heart
failure, sepsis, neuromyelitis optica, glioblastoma, fibromyalgia,
multiple sclerosis, or migraines comprising administering an
effective amount of an inhibitor of AQP4, e.g, a compound binding
to AQP4, to a patient in need thereof, e.g., wherein the inhibitor
of AQP4 is selected from phenylbenzamides, e.g. niclosamide or a
compound of Formula I or formula 1a as hereinbefore described,
e.g., any of the compounds identified in Method 1-1.28 above, for
example [0247] 4. [0248] 4.1. Method 4 wherein the condition to be
treated or controlled is retinal ischemia or other diseases of the
eye associated with abnormalities in intraocular pressure and/or
tissue hydration. [0249] 4.2. Method 4 wherein the condition to be
treated or controlled is myocardial ischemia. [0250] 4.3. Method 4
wherein the condition to be treated or controlled is myocardial
ischemia/reperfusion injury. [0251] 4.4. Method 4 wherein the
condition to be treated or controlled is myocardial infarction.
[0252] 4.5. Method 4 wherein the condition to be treated or
controlled is myocardial hypoxia. [0253] 4.6. Method 4 wherein the
condition to be treated or controlled is congestive heart failure.
[0254] 4.7. Method 4 wherein the condition to be treated or
controlled is sepsis. [0255] 4.8. Method 4 wherein the condition to
be treated or controlled is neuromyelitis optica. [0256] 4.9.
Method 4 wherein the condition to be treated or controlled is a
migraine. [0257] 4.10. Method 4 wherein the condition to be treated
or controlled is glioblastoma. [0258] 4.11. Method 4 wherein the
condition to be treated or controlled is fibromyalgia. [0259] 4.12.
Method 4 wherein the condition to be treated or controlled is
multiple sclerosis. [0260] 4.13. Any of Method 4, et seq. wherein
the AQP4 inhibitor inhibits AQP4 activity by at least 50% at
concentrations of 10 micromolar or less, for example inhibits APQ4
activity by at least 50% at concentrations of 10 micromolar or less
in an aquaporin-mediated cell volume change assay, e.g., is active
in any of the assays of Method 10, et seq. infra. [0261] 4.14. Any
of Method 4, et seq. wherein the AQP4 inhibitor is administered
orally. [0262] 4.15. Any of Method 4, et seq. wherein the AQP4
inhibitor is administered parenterally. [0263] 4.16. Method 4.15
wherein the AQP4 inhibitor is administered intravenously. [0264]
4.17. Any of Method 4, et seq. wherein the patient is human. [0265]
4.18. Any of Method 4, et seq. wherein the onset of action of any
of the compounds identified in Methods 1-1.28 is fairly rapid.
[0266] In a further embodiment, the invention provides a method
(Method 5) of treating or controlling a disease or condition
mediated by an aquaporin comprising administering to a patient in
need thereof a phenylbenzamide, e.g. niclosamide or a compound of
Formula I or formula 1a as hereinbefore described, e.g., any of the
compounds identified in Method 1-1.28 above, in an amount effective
to inhibit the aquaporin, for example [0267] 5. [0268] 5.1. Method
5 wherein the aquaporin is AQP4. [0269] 5.2. Method 5 or 5.1
wherein the condition to be treated or controlled is selected from
edema, e.g. edema of the brain or spinal cord, e.g., cerebral
edema, e.g. cerebral edema consequent to head trauma, ischemic
stroke, glioma, meningitis, acute mountain sickness, epileptic
seizures, infections, metabolic disorders, water intoxication,
hepatic failure, hepatic encephalopathy, or diabetic ketoacidosis
or, e.g., spinal cord edema, e.g., spinal cord edema consequent to
spinal cord trauma, e.g., spinal cord compression. [0270] 5.3.
Method 5.2 further comprising a treatment selected from one or more
of the following: optimal head and neck positioning to facilitate
venous outflow, e.g. head elevation 30.degree.; avoidance of
dehydration; systemic hypotension; maintenance of normothermia or
hypothermia; aggressive measures; osmotherapy, e.g., using mannitol
or hypertonic saline; hyperventilation; therapeutic pressor therapy
to enhance cerebral perfusion; administration of barbiturates to
reduce of cerebral metabolism (CMO.sub.2); hemicraniectomy;
administration of aspirin; administration of amantadine;
intravenous thrombolysis (e.g. using rtPA); mechanical clot
removal; angioplasty; and/or stents. [0271] 5.4. Any of Method 5,
et seq. wherein the patient is at elevated risk of cerebral edema,
e.g., due to head trauma, ischemic stroke, glioma, meningitis,
acute mountain sickness, epileptic seizure, infection, metabolic
disorder, water intoxication, hepatic failure, hepatic
encephalopathy, or diabetic ketoacidosis. [0272] 5.5. Any of Method
5, et seq. wherein the patient has suffered a stroke, head injury,
or spinal injury. [0273] 5.6. Any of Method 5, et seq. wherein the
patient has suffered a stroke, head injury or spinal injury within
12 hours, e.g. within 6 hours, preferably within 3 hours of
commencing treatment. [0274] 5.7. Any of Method 5, et seq. wherein
the patient is at elevated risk of suffering a stroke, head injury
or spinal injury, e.g., in combat or in an athletic competition.
[0275] 5.8. Any of Method 5, et seq. wherein the patient already
has cerebral edema. [0276] 5.9. Any of Method 5, et seq. wherein
the condition to be treated or controlled is cerebral edema
consequent to a stroke or a traumatic brain injury. [0277] 5.10.
Any of Method 5, et seq. wherein the condition to be treated or
controlled is cerebral edema consequent to a middle cerebral artery
stroke. [0278] 5.11. Any of Method 5, et seq. wherein the condition
to be treated or controlled is cerebral edema consequent to a
closed head trauma. [0279] 5.12. Any of Methods 5-5.4 wherein the
condition to be treated or controlled is cerebral edema consequent
to an epileptic seizure. [0280] 5.13. Any of Methods 5-5.4 wherein
the condition to be treated or controlled is cerebral edema
consequent to an infection. [0281] 5.14. Any of Methods 5-5.4
wherein the condition to be treated or controlled is cerebral edema
consequent to a metabolic disorder. [0282] 5.15. Any of Methods
5-5.4 wherein the condition to be treated or controlled is cerebral
edema consequent to glioma. [0283] 5.16. Any of Methods 5-5.4
wherein the condition to be treated or controlled is cerebral edema
consequent to meningitis, acute mountain sickness, or water
intoxication. [0284] 5.17. Any of Methods 5-5.4 wherein the
condition to be treated or controlled is cerebral edema consequent
to hepatic failure, hepatic encephalopathy, or diabetic
ketoacidosis. [0285] 5.18. Any of Methods 5-5.3 wherein the
condition to be treated or controlled is cerebral edema consequent
to an abscess. [0286] 5.19. Any of Methods 5-5.3 wherein the
condition to be treated or controlled is cerebral edema consequent
to eclampsia. [0287] 5.20. Any of Methods 5-5.3 wherein the
condition to be treated or controlled is cerebral edema consequent
to Creutzfeldt-Jakob disease. [0288] 5.21. Any of Methods 5-5.3
wherein the condition to be treated or controlled is cerebral edema
consequent to lupus cerebritis. [0289] 5.22. Any of Methods 5-5.3
wherein the condition to be treated or controlled is edema
consequent to hypoxia, e.g., general systemic hypoxia, e.g.,
hypoxia caused by an interruption of blood perfusion, for example
wherein the edema is cerebral edema consequent to hypoxia caused by
cardiac arrest, stroke, or other interruption of blood perfusion to
the brain, or wherein the edema is cardiac edema consequent to
cardiac ischemia or other interruption of blood flow to the heart.
[0290] 5.23. Any of Methods 5-5.3 wherein the condition to be
treated or controlled is cerebral consequent to microgravity and/or
radiation exposure, e.g., exposure from space flight or from
working with radioactive materials or from working in radioactive
areas and/or optic nerve edema consequent to microgravity exposure,
e.g., exposure from space flight or from working with radioactive
materials or from working in radioactive areas. [0291] 5.24. Any of
Methods 5-5.3 wherein the condition to be treated or controlled is
cerebral edema consequent to invasive central nervous system
procedures, e.g., neurosurgery, endovascular clot removal, spinal
tap, aneurysm repair, or deep brain stimulation. [0292] 5.25.
Method 5.23 or 5.24 wherein the patient is at elevated risk of
edema, e.g., due to microgravity and/or radiation exposure,
neurosurgery, endovascular clot removal, spinal tap, aneurysm
repair, or deep brain stimulation. [0293] 5.26. Method 5.23 or 5.24
wherein the patient already has edema. [0294] 5.27. Any of Methods
5, et seq. wherein the edema is cytotoxic cerebral edema or is
primarily cytotoxic cerebral edema. [0295] 5.28. Any of Methods
5-5.17 or 5.22 wherein the edema is cytotoxic cerebral edema or is
primarily cytotoxic cerebral edema. [0296] 5.29. Method 5 or 5.1
wherein the condition to be treated or controlled is spinal cord
edema, e.g., spinal cord edema consequent to spinal cord trauma,
e.g., spinal cord compression. [0297] 5.30. Method 5.29 wherein the
condition to be treated or controlled is spinal cord edema
consequent to spinal cord compression. [0298] 5.31. Any of Methods
5-5.2 wherein the condition to be treated or controlled is retinal
edema. [0299] 5.32. Any of Methods 5-5.2 wherein the condition to
be treated or controlled is pulmonary edema. [0300] 5.33. Method 5
or 5.1 wherein the condition to be treated or controlled is
epilepsy. [0301] 5.34. Method 5 or 5.1 wherein the condition to be
treated or controlled is retinal ischemia or other diseases of the
eye associated with abnormalities in intraocular pressure and/or
tissue hydration. [0302] 5.35. Method 5 or 5.1 wherein the
condition to be treated or controlled is myocardial ischemia.
[0303] 5.36. Method 5 or 5.1 wherein the condition to be treated or
controlled is myocardial ischemia/reperfusion injury. [0304] 5.37.
Method 5 or 5.1 wherein the condition to be treated or controlled
is myocardial infarction. [0305] 5.38. Method 5 or 5.1 wherein the
condition to be treated or controlled is myocardial hypoxia. [0306]
5.39. Method 5 or 5.1 wherein the condition to be treated or
controlled is congestive heart failure. [0307] 5.40. Method 5 or
5.1 wherein the condition to be treated or controlled is sepsis.
[0308] 5.41. Method 5 or 5.1 wherein the condition to be treated or
controlled is a migraine. [0309] 5.42. Method 5 or 5.1 wherein the
condition to be treated or controlled is glioblastoma. [0310] 5.43.
Method 5 or 5.1 wherein the condition to be treated or controlled
is fibromyalgia. [0311] 5.44. Method 5 or 5.1 wherein the condition
to be treated or controlled is multiple sclerosis. [0312] 5.45.
Method 5 wherein the aquaporin is AQP2. [0313] 5.46. Method 5 or
5.45 wherein the condition to be treated is hyponatremia or
excessive fluid retention, e.g., consequent to heart failure (HF),
for example congestive heart failure, liver cirrhosis, nephrotic
disorder, syndrome of inappropriate antidiuretic hormone secretion
(SIADH), or infertility treatment, e.g., infertility treatment.
[0314] 5.47. Method 5 or 5.45 wherein the condition to be or
controlled is ovarian hyperstimulation syndrome. [0315] 5.48.
Method 5 or 5.45-5.47 further comprising one or more of restriction
of dietary sodium, fluid and/or alcohol; and/or administration of
one or more diuretics, vasopressin receptor antagonists,
angiotensin converting enzyme (ACE) inhibitors, aldosterone
inhibitors, angiotensin receptor blockers (ARBs), beta-adrenergic
antagonists (beta-blockers), and/or digoxin. [0316] 5.49. Any of
Method 5, et seq. wherein the compound of Formula I or formula 1a
inhibits aquaporin activity, e.g., AQP2 and/or AQP4 activity, by at
least 50% at concentrations of 10 micromolar or less, for example
inhibits APQ2 and/or AQP4 activity by at least 50% at
concentrations of 10 micromolar or less in an aquaporin-mediated
cell volume change assay, e.g., is active in any of the assays of
Method 10, et seq. infra. [0317] 5.50. Any of Method 5, et seq.
wherein the duration of treatment with the phenylbenzamide is less
than 21 days, e.g., less than 2 weeks, e.g., one week or less.
[0318] 5.51. Any of Method 5, et seq. wherein the niclosamide or
the compound of Formula I or formula 1a is administered orally.
[0319] 5.52. Any of Method 5, et seq. wherein the niclosamide or
the compound of Formula I or formula 1a is administered
parenterally. [0320] 5.53. Method 5.52 wherein the niclosamide or
the compound of Formula I or formula 1a is administered
intravenously. [0321] 5.54. Any of Method 5, et seq. wherein the
patient is human. [0322] 5.55. Any of Method 5, et seq. wherein the
onset of action of any of the compounds identified in Methods
1-1.28 is fairly rapid.
[0323] In a further embodiment, the invention provides a method
(Method 6) of inhibiting an aquaporin comprising contacting the
aquaporin with an effective amount of a phenylbenzamide, e.g.
niclosamide or a compound of Formula I or formula 1a as
hereinbefore described, e.g., any of the compounds identified in
Method 1-1.28 above, for example [0324] 6. [0325] 6.1. Method 6
wherein the aquaporin is inhibited in vivo. [0326] 6.2. Method 6
wherein the aquaporin is inhibited in vitro. [0327] 6.3. Any of
Methods 6, et seq. wherein the aquaporin is AQP4. [0328] 6.4. Any
of Method 6, et seq. wherein the aquaporin is AQP2. [0329] 6.5. Any
of Method 6, et seq. wherein the compound of Formula I or formula
1a inhibits aquaporin activity, e.g., AQP2 and/or AQP4 activity, by
at least 50% at concentrations of 10 micromolar or less, for
example inhibits APQ2 and/or AQP4 activity by at least 50% at
concentrations of 10 micromolar or less in an aquaporin-mediated
cell volume change assay, e.g., is active in any of the assays of
Method 10, et seq. infra. [0330] 6.6. Method 6.1 wherein the
niclosamide or the compound of Formula I or formula 1a is
administered orally. [0331] 6.7. Method 6.1 wherein the niclosamide
or the compound of Formula I or formula 1a is administered
parenterally. [0332] 6.8. Method of 6.7 wherein the niclosamide or
the compound of Formula I or formula 1a is administered
intravenously.
[0333] In a further embodiment, the invention provides a method
(Method 7) to inhibit an aquaporin in a patient suffering from a
disease or condition mediated by an aquaporin comprising
administering an effective amount of a phenylbenzamide, e.g.
niclosamide or a compound of Formula I or formula 1a as
hereinbefore described, e.g., any of the compounds identified in
Method 1-1.28 above, to inhibit the aquaporin. [0334] 7. [0335]
7.1. Method 7 wherein the aquaporin is AQP4. [0336] 7.2. Method 7
or 7.1 wherein the condition to be treated or controlled is
selected from edema, e.g. edema of the brain or spinal cord, e.g.,
cerebral edema, e.g. cerebral edema consequent to head trauma,
ischemic stroke, glioma, meningitis, acute mountain sickness,
epileptic seizure, infection, metabolic disorder, water
intoxication, hepatic failure, hepatic encephalopathy, or diabetic
ketoacidosis or, e.g., spinal cord edema, e.g., spinal cord edema
consequent to spinal cord trauma, e.g., spinal cord compression.
[0337] 7.3. Method 7.2 further comprising a treatment selected from
one or more of the following: optimal head and neck positioning to
facilitate venous outflow, e.g. head elevation 30.degree.;
avoidance of dehydration; systemic hypotension; maintenance of
normothermia or hypothermia; aggressive measures; osmotherapy,
e.g., using mannitol or hypertonic saline; hyperventilation;
therapeutic pressor therapy to enhance cerebral perfusion;
administration of barbiturates to reduce of cerebral metabolism
(CMO.sub.2); hemicraniectomy; administration of aspirin;
administration of amantadine; intravenous thrombolysis (e.g. using
rtPA); mechanical clot removal; angioplasty; and/or stents. [0338]
7.4. Any of Method 7, et seq. wherein the patient is at elevated
risk of cerebral edema, e.g., due to head trauma, ischemic stroke,
glioma, meningitis, acute mountain sickness, epileptic seizure,
infection, metabolic disorder, water intoxication, hepatic failure,
hepatic encephalopathy, or diabetic ketoacidosis. [0339] 7.5. Any
of Method 7, et seq. wherein the patient has suffered a stroke,
head injury, or spinal injury. [0340] 7.6. Any of Method 7, et seq.
wherein the patient has suffered a stroke, head injury or spinal
injury within 12 hours, e.g. within 6 hours, preferably within 3
hours of commencing treatment. [0341] 7.7. Any of Method 7, et seq.
wherein the patient is at elevated risk of suffering a stroke, head
injury or spinal injury, e.g., in combat or in an athletic
competition. [0342] 7.8. Any of Method 7, et seq. wherein the
patient already has cerebral edema. [0343] 7.9. Any of Method 7, et
seq. wherein the condition to be treated or controlled is cerebral
edema consequent to a stroke or a traumatic brain injury. [0344]
7.10. Any of Method 7, et seq. wherein the condition to be treated
or controlled is cerebral edema consequent to a middle cerebral
artery stroke. [0345] 7.11. Any of Method 7, et seq. wherein the
condition to be treated or controlled is cerebral edema consequent
to a closed head trauma. [0346] 7.12. Any of Methods 7-7.4 wherein
the condition to be treated or controlled is cerebral edema
consequent to an epileptic seizure. [0347] 7.13. Any of Methods
7-7.4 wherein the condition to be treated or controlled is cerebral
edema consequent an infection. [0348] 7.14. Any of Methods 7-7.4
wherein the condition to be treated or controlled is cerebral edema
consequent to a metabolic disorder. [0349] 7.15. Any of Methods
7-7.4 wherein the condition to be treated or controlled is cerebral
edema consequent to glioma. [0350] 7.16. Any of Methods 7-7.4
wherein the condition to be treated or controlled is cerebral edema
consequent to meningitis, acute mountain sickness, or water
intoxication. [0351] 7.17. Any of Methods 7-7.4 wherein the
condition to be treated or controlled is cerebral edema consequent
to hepatic failure, hepatic encephalopathy, or diabetic
ketoacidosis. [0352] 7.18. Any of Methods 7-7.3 wherein the
condition to be treated or controlled is cerebral edema consequent
to an abscess. [0353] 7.19. Any of Methods 7-7.3 wherein the
condition to be treated or controlled is cerebral edema consequent
to eclampsia. [0354] 7.20. Any of Methods 7-7.3 wherein the
condition to be treated or controlled is cerebral edema consequent
to Creutzfeldt-Jakob disease. [0355] 7.21. Any of Methods 7-7.3
wherein the condition to be treated or controlled is cerebral edema
consequent to lupus cerebritis. [0356] 7.22. Any of Methods 7-7.3
wherein the condition to be treated or controlled is edema
consequent to hypoxia, e.g., general systemic hypoxia, e.g.,
hypoxia caused by an interruption of blood perfusion, for example
wherein the edema is cerebral edema consequent to hypoxia caused by
cardiac arrest, stroke, or other interruption of blood perfusion to
the brain, or wherein the edema is cardiac edema consequent to
cardiac ischemia or other interruption of blood flow to the heart.
[0357] 7.23. Any of Methods 7-7.3 wherein the condition to be
treated or controlled is cerebral consequent to microgravity and/or
radiation exposure, e.g., exposure from space flight or from
working with radioactive materials or from working in radioactive
areas and/or optic nerve edema, e.g, optic nerve edema consequent
to microgravity and/or radiation exposure, e.g., exposure from
space flight or from working with radioactive materials or from
working in radioactive area, e.g., optic nerve edema. [0358] 7.24.
Any of Methods 7-7.3 wherein the condition to be treated or
controlled is cerebral edema consequent to invasive central nervous
system procedures, e.g., neurosurgery, endovascular clot removal,
spinal tap, aneurysm repair, or deep brain stimulation. [0359]
7.25. Method 7.23 or 7.24 wherein the patient is at elevated risk
of edema, e.g., due to microgravity and/or radiation exposure,
neurosurgery, endovascular clot removal, spinal tap, aneurysm
repair, or deep brain stimulation. [0360] 7.26. Method 7.23 or 7.24
wherein the patient already has edema. [0361] 7.27. Any of Methods
7, et seq. wherein the edema is cytotoxic cerebral edema or is
primarily cytotoxic cerebral edema. [0362] 7.28. Any of Methods
7-7.17 or 7.22 wherein the edema is cytotoxic cerebral edema or is
primarily cytotoxic cerebral edema. [0363] 7.29. Any of Methods
7-7.2 wherein the condition to be treated or controlled is spinal
cord edema, e.g., spinal cord edema consequent to spinal cord
trauma, e.g., spinal cord compression. [0364] 7.30. Method 7.29
wherein the condition to be treated or controlled is spinal cord
edema consequent to spinal cord compression. [0365] 7.31. Any of
Methods 7-7.2 wherein the condition to be treated or controlled is
retinal edema. [0366] 7.32. Any of Methods 7-7.2 wherein the
condition to be treated or controlled is pulmonary edema. [0367]
7.33. Method 7 or 7.1 wherein the condition to be treated or
controlled is epilepsy. [0368] 7.34. Method 7 or 7.1 wherein the
condition to be treated or controlled is retinal ischemia or other
diseases of the eye associated with abnormalities in intraocular
pressure and/or tissue hydration. [0369] 7.35. Method 7 or 7.1
wherein the condition to be treated or controlled is myocardial
ischemia. [0370] 7.36. Method 7 or 7.1 wherein the condition to be
treated or controlled is myocardial ischemia/reperfusion injury.
[0371] 7.37. Method 7 or 7.1 wherein the condition to be treated or
controlled is myocardial infarction. [0372] 7.38. Method 7 or 7.1
wherein the condition to be treated or controlled is myocardial
hypoxia. [0373] 7.39. Method 7 or 7.1 wherein the condition to be
treated or controlled is congestive heart failure. [0374] 7.40.
Method 7 or 7.1 wherein the condition to be treated or controlled
is sepsis. [0375] 7.41. Method 7 or 7.1 wherein the condition to be
treated or controlled is a migraine. [0376] 7.42. Method 7 or 7.1
wherein the condition to be treated or controlled is glioblastoma.
[0377] 7.43. Method 7 or 7.1 wherein the condition to be treated or
controlled is fibromyalgia. [0378] 7.44. Method 7 or 7.1 wherein
the condition to be treated or controlled is multiple sclerosis.
[0379] 7.45. Method 7 wherein the aquaporin is AQP2. [0380] 7.46.
Method 7 or 7.45 wherein the condition to be treated is
hyponatremia or excessive fluid retention, e.g., consequent to
heart failure (HF), for example congestive heart failure, liver
cirrhosis, nephrotic disorder, syndrome of inappropriate
antidiuretic hormone secretion (SIADH), or infertility treatment,
e.g., infertility treatment. [0381] 7.47. Method 7 or 7.45 wherein
the condition to be treated is ovarian hyperstimulation syndrome.
[0382] 7.48. Method 7 or 7.45-7.47 further comprising one or more
of restriction of dietary sodium, fluid and/or alcohol; and/or
administration of one or more diuretics, vasopressin receptor
antagonists, angiotensin converting enzyme (ACE) inhibitors,
aldosterone inhibitors, angiotensin receptor blockers (ARBs),
beta-adrenergic antagonists (beta-blockers), and/or digoxin. [0383]
7.49. Any of Method 7, et seq. wherein the compound of Formula I or
formula 1a inhibits aquaporin activity, e.g., AQP2 and/or AQP4
activity, by at least 50% at concentrations of 10 micromolar or
less, for example inhibits APQ2 and/or AQP4 activity by at least
50% at concentrations of 10 micromolar or less in an
aquaporin-mediated cell volume change assay, e.g., is active in any
of the assays of Method 10, et seq. infra. [0384] 7.50. Any of
Method 7, et seq. wherein the duration of treatment with the
phenylbenzamide is less than 21 days, e.g., less than 2 weeks,
e.g., one week or less. [0385] 7.51. Any of Method 7, et seq.
wherein the niclosamide or compound of Formula I or formula 1a is
administered orally. [0386] 7.52. Any of Method 7, et seq. wherein
the niclosamide or compound of Formula I or formula 1a is
administered parenterally. [0387] 7.53. Method 7.52 wherein the
niclosamide or compound of Formula I or formula 1a is administered
intravenously. [0388] 7.54. Any of Method 7, et seq. wherein the
patient is human. [0389] 7.55. Any of Method 7, et seq. wherein the
onset of action of any of the compounds identified in Methods
1-1.28 is fairly rapid.
[0390] In a further embodiment, the invention provides a
pharmaceutical composition comprising a phenylbenzamide, e.g.
niclosamide or a compound of Formula I or formula 1a as
hereinbefore described, e.g., any of the compounds identified in
Methods 1-1.28 above, for use (Use 8) to inhibit an aquaporin in a
patient suffering from a disease or condition mediated by the
aquaporin. For example, for use in any of the foregoing methods.
[0391] 8. [0392] 8.1. Use 8 wherein the aquaporin is AQP4. [0393]
8.2. Use 8 or 8.1 wherein the condition to be treated or controlled
is selected from edema, e.g. edema of the brain or spinal cord,
e.g., cerebral edema, e.g. cerebral edema consequent to head
trauma, ischemic stroke, glioma, meningitis, acute mountain
sickness, epileptic seizure, infection, metabolic disorder, water
intoxication, hepatic failure, hepatic encephalopathy, or diabetic
ketoacidosis or, e.g., spinal cord edema, e.g., spinal cord edema
consequent to spinal cord trauma, e.g., spinal cord compression.
[0394] 8.3. Use 8.2 further comprising a treatment selected from
one or more of the following: optimal head and neck positioning to
facilitate venous outflow, e.g. head elevation 30.degree.;
avoidance of dehydration; systemic hypotension; maintenance of
normothermia or hypothermia; aggressive measures; osmotherapy,
e.g., using mannitol or hypertonic saline; hyperventilation;
therapeutic pressor therapy to enhance cerebral perfusion;
administration of barbiturates to reduce of cerebral metabolism
(CMO.sub.2); hemicraniectomy; administration of aspirin;
administration of amantadine; intravenous thrombolysis (e.g. using
rtPA); mechanical clot removal; angioplasty; and/or stents. [0395]
8.4. Any of Use 8, et seq. wherein the patient is at elevated risk
of cerebral edema, e.g., due to head trauma, ischemic stroke,
glioma, meningitis, acute mountain sickness, epileptic seizure,
infection, metabolic disorder, water intoxication, hepatic failure,
hepatic encephalopathy, or diabetic ketoacidosis. [0396] 8.5. Any
of Use 8, et seq. wherein the patient has suffered a stroke, head
injury, or spinal injury. [0397] 8.6. Any of Use 8, et seq. wherein
the patient has suffered a stroke, head injury or spinal injury
within 12 hours, e.g. within 6 hours, preferably within 3 hours of
commencing treatment. [0398] 8.7. Any of Use 8, et seq. wherein the
patient is at elevated risk of suffering a stroke, head injury or
spinal injury, e.g., in combat or in an athletic competition.
[0399] 8.8. Any of Use 8, et seq. wherein the patient already has
cerebral edema. [0400] 8.9. Any of Use 8, et seq. wherein the
condition to be treated or controlled is cerebral edema consequent
to a stroke or a traumatic brain injury. [0401] 8.10. Any of Use 8,
et seq. wherein the condition to be treated or controlled is
cerebral edema consequent to a middle cerebral artery stroke.
[0402] 8.11. Any of Use 8, et seq. wherein the condition to be
treated or controlled is cerebral edema consequent to a closed head
trauma. [0403] 8.12. Any of Uses 8-8.4 wherein the condition to be
treated or controlled is cerebral edema consequent to an epileptic
seizure. [0404] 8.13. Any of Uses 8-8.4 wherein the condition to be
treated or controlled is cerebral edema consequent to an infection.
[0405] 8.14. Any of Uses 8-8.4 wherein the condition to be treated
or controlled is cerebral edema consequent to a metabolic disorder.
[0406] 8.15. Any of Uses 8-8.4 wherein the condition to be treated
or controlled is cerebral edema consequent to glioma. [0407] 8.16.
Any of Uses 8-8.4 wherein the condition to be treated or controlled
is cerebral edema consequent to meningitis, acute mountain
sickness, or water intoxication. [0408] 8.17. Any of Uses 8-8.4
wherein the condition to be treated or controlled is cerebral edema
consequent to hepatic failure, hepatic encephalopathy, or diabetic
ketoacidosis. [0409] 8.18. Any of the Uses 8-8.3 wherein the
condition to be treated or controlled is cerebral edema consequent
to an abscess. [0410] 8.19. Any of the Uses 8-8.3 wherein the
condition to be treated or controlled is cerebral edema consequent
to eclampsia. [0411] 8.20. Any of Uses 8-8.3 wherein the condition
to be treated or controlled is cerebral edema consequent to
Creutzfeldt-Jakob disease. [0412] 8.21. Any of Uses 8-8.3 wherein
the condition to be treated or controlled is cerebral edema
consequent lupus cerebritis. [0413] 8.22. Any of Uses 8-8.3 wherein
the condition to be treated or controlled is edema consequent to
hypoxia, e.g., general systemic hypoxia, e.g., hypoxia caused by an
interruption of blood perfusion, for example wherein the edema is
cerebral edema consequent to hypoxia caused by cardiac arrest,
stroke, or other interruption of blood perfusion to the brain, or
wherein the edema is cardiac edema consequent to cardiac ischemia
or other interruption of blood flow to the heart. [0414] 8.23. Any
of Uses 8-8.3 wherein the condition to be treated or controlled is
cerebral consequent to microgravity and/or radiation exposure,
e.g., exposure from space flight or from working with radioactive
materials or from working in radioactive areas and/or optic nerve
edema, e.g., optic nerve edema consequent to microgravity and/or
radiation exposure, e.g., exposure from space flight or from
working with radioactive materials or from working in radioactive
areas, e.g., optic nerve edema. [0415] 8.24. Any of Uses 8-8.3
wherein the condition to be treated or controlled is cerebral edema
consequent to invasive central nervous system procedures, e.g.,
neurosurgery, endovascular clot removal, spinal tap, aneurysm
repair, or deep brain stimulation. [0416] 8.25. Use 8.23 or 8.24
wherein the patient is at elevated risk of edema, e.g., due to
microgravity exposure and/or radiation, neurosurgery, endovascular
clot removal, spinal tap, aneurysm repair, or deep brain
stimulation. [0417] 8.26. Use 8.23 or 8.24 wherein the patient
already has edema. [0418] 8.27. Any of Uses 8, et seq. wherein the
edema is cytotoxic cerebral edema or is primarily cytotoxic
cerebral edema. [0419] 8.28. Any of Uses 8-8.17 or 8.22 wherein the
edema is cytotoxic cerebral edema or is primarily cytotoxic
cerebral edema. [0420] 8.29. Any of Uses 8-8.2 wherein the
condition to be treated or controlled is spinal cord edema, e.g.,
spinal cord edema consequent to spinal cord trauma, e.g., spinal
cord compression. [0421] 8.30. Use 8.29 wherein the condition to be
treated or controlled is spinal cord edema consequent to spinal
cord compression. [0422] 8.31. Any of Uses 8-8.2 wherein the
condition to be treated or controlled is retinal edema. [0423]
8.32. Any of Uses 8-8.2 wherein the condition to be treated or
controlled is pulmonary edema. [0424] 8.33. Use 8 or 8.1 wherein
the condition to be treated or controlled is epilepsy. [0425] 8.34.
Use 8 or 8.1 wherein the condition to be treated or controlled is
retinal ischemia or other diseases of the eye associated with
abnormalities in intraocular pressure and/or tissue hydration.
[0426] 8.35. Use 8 or 8.1 wherein the condition to be treated or
controlled is myocardial ischemia. [0427] 8.36. Use 8 or 8.1
wherein the condition to be treated or controlled is myocardial
ischemia/reperfusion injury. [0428] 8.37. Use 8 or 8.1 wherein the
condition to be treated or controlled is myocardial infarction.
[0429] 8.38. Use 8 or 8.1 wherein the condition to be treated or
controlled is myocardial hypoxia. [0430] 8.39. Use 8 or 8.1 wherein
the condition to be treated or controlled is congestive heart
failure. [0431] 8.40. Use 8 or 8.1 wherein the condition to be
treated or controlled is sepsis. [0432] 8.41. Use 8 or 8.1 wherein
the condition to be treated or controlled is a migraine. [0433]
8.42. Use 8 or 8.1 wherein the condition to be treated or
controlled is glioblastoma. [0434] 8.43. Use 8 or 8.1 wherein the
condition to be treated or controlled is fibromyalgia. [0435] 8.44.
Use 8 or 8.1 wherein the condition to be treated or controlled is
multiple sclerosis. [0436] 8.45. Use 8 wherein the aquaporin is
AQP2. [0437] 8.46. Use 8 or 8.45 wherein the condition to be
treated is hyponatremia or excessive fluid retention, e.g.,
consequent to heart failure (HF), for example congestive heart
failure, liver cirrhosis, nephrotic disorder, syndrome of
inappropriate antidiuretic hormone secretion (SIADH), or
infertility treatment, e.g., infertility treatment. [0438] 8.47.
Use 8 or 8.45 wherein the condition to be treated is ovarian
hyperstimulation syndrome. [0439] 8.48. Use 8 or 8.45-8.47 further
comprising one or more of restriction of dietary sodium, fluid
and/or alcohol; and/or administration of one or more diuretics,
vasopressin receptor antagonists, angiotensin converting enzyme
(ACE) inhibitors, aldosterone inhibitors, angiotensin receptor
blockers (ARBs), beta-adrenergic antagonists (beta-blockers),
and/or digoxin. [0440] 8.49. Any of Use 8, et seq. wherein the
compound of Formula I or formula 1a inhibits aquaporin activity,
e.g., AQP2 and/or AQP4 activity, by at least 50% at concentrations
of 10 micromolar or less, for example inhibits APQ2 and/or AQP4
activity by at least 50% at concentrations of 10 micromolar or less
in an aquaporin-mediated cell volume change assay, e.g., is active
in any of the assays of Method 10, et seq. infra. [0441] 8.50. Any
of Use 8, et seq. wherein the duration of treatment with the
phenylbenzamide is less than 21 days, e.g., less than 2 weeks,
e.g., one week or less. [0442] 8.51. Any of Use 8, et seq. wherein
the pharmaceutical composition is administered orally. [0443] 8.52.
Any of Use 8, et seq. wherein the pharmaceutical composition is
administered parenterally. [0444] 8.53. Use 8.52 wherein the
pharmaceutical composition is administered intravenously. [0445]
8.54. Any of Use 8, et seq. wherein the patient is human. [0446]
8.55. Any of Use 8, et seq. wherein the onset of action of the
pharmaceutical composition is fairly rapid.
[0447] In a further embodiment, the invention provides use (Use 9)
of a phenylbenzamide, e.g. niclosamide or a compound of Formula I
or formula 1a as hereinbefore described, e.g., any of the compounds
identified in Methods 1-1.28 above, in the manufacture of a
medicament for treating or controlling a disease or condition
mediated by an aquaporin wherein the medicament comprises the
phenylbenzamide in an amount effective to inhibit the aquaporin.
For example, for use in any of the foregoing methods. [0448] 9.
[0449] 9.1. Use 9 wherein the aquaporin is AQP4. [0450] 9.2. Any of
Use 9 or 9.1 wherein the condition to be treated or controlled is
selected from edema, e.g. edema of the brain or spinal cord, e.g.,
cerebral edema, e.g. cerebral edema consequent to head trauma,
ischemic stroke, glioma, meningitis, acute mountain sickness,
epileptic seizure, infection, metabolic disorder, water
intoxication, hepatic failure, hepatic encephalopathy, or diabetic
ketoacidosis or, e.g., spinal cord edema, e.g., spinal cord edema
consequent to spinal cord trauma, e.g., spinal cord compression.
[0451] 9.3. Use 9.2 further comprising a treatment selected from
one or more of the following: optimal head and neck positioning to
facilitate venous outflow, e.g. head elevation 30.degree.;
avoidance of dehydration; systemic hypotension; maintenance of
normothermia or hypothermia; aggressive measures; osmotherapy,
e.g., using mannitol or hypertonic saline; hyperventilation;
therapeutic pressor therapy to enhance cerebral perfusion;
administration of barbiturates to reduce of cerebral metabolism
(CMO.sub.2); hemicraniectomy; administration of aspirin;
administration of amantadine; intravenous thrombolysis (e.g. using
rtPA); mechanical clot removal; angioplasty; and/or stents. [0452]
9.4. Any of Use 9, et seq. wherein the patient is at elevated risk
of cerebral edema, e.g., due to head trauma, ischemic stroke,
glioma, meningitis, acute mountain sickness, epileptic seizure,
infection, metabolic disorder, water intoxication, hepatic failure,
hepatic encephalopathy, or diabetic ketoacidosis. [0453] 9.5. Any
of Use 9, et seq. wherein the patient has suffered a stroke, head
injury, or spinal injury. [0454] 9.6. Any of Use 9, et seq. wherein
the patient has suffered a stroke, head injury or spinal injury
within 12 hours, e.g. within 6 hours, preferably within 3 hours of
commencing treatment. [0455] 9.7. Any of Use 9, et seq. wherein the
patient is at elevated risk of suffering a stroke, head injury or
spinal injury, e.g., in combat or in an athletic competition.
[0456] 9.8. Any of Use 9, et seq. wherein the patient already has
cerebral edema. [0457] 9.9. Any of Use 9, et seq. wherein the
condition to be treated or controlled is cerebral edema consequent
to a stroke or a traumatic brain injury. [0458] 9.10. Any of Use 9,
et seq. wherein the condition to be treated or controlled is
cerebral edema consequent to a middle cerebral artery stroke.
[0459] 9.11. Any of Use 9, et seq. wherein the condition to be
treated or controlled is cerebral edema consequent to a closed head
trauma. [0460] 9.12. Any of Uses 9-9.4 wherein the condition to be
treated or controlled is cerebral edema consequent to an epileptic
seizure. [0461] 9.13. Any of Uses 9-9.4 wherein the condition to be
treated or controlled is cerebral edema consequent to an infection.
[0462] 9.14. Any of Uses 9-9.4 wherein the condition to be treated
or controlled is cerebral edema consequent to a metabolic disorder.
[0463] 9.15. Any of Uses 9-9.4 wherein the condition to be treated
or controlled is cerebral edema consequent to glioma. [0464] 9.16.
Any of Uses 9-9.4 wherein the condition to be treated or controlled
is cerebral edema consequent to meningitis, acute mountain
sickness, or water intoxication. [0465] 9.17. Any of Uses 9-9.4
wherein the condition to be treated or controlled is cerebral edema
consequent to hepatic failure, hepatic encephalopathy, or diabetic
ketoacidosis. [0466] 9.18. Any of Uses 9-9.3 wherein the condition
to be treated or controlled is cerebral edema consequent to an
abscess. [0467] 9.19. Any of Uses 9-9.3 wherein the condition to be
treated or controlled is cerebral edema consequent to eclampsia.
[0468] 9.20. Any of Uses 9-9.3 wherein the condition to be treated
or controlled is cerebral edema consequent to Creutzfeldt-Jakob
disease. [0469] 9.21. Any of Uses 9-9.3 wherein the condition to be
treated or controlled is cerebral edema consequent to lupus
cerebritis. [0470] 9.22. Any of Uses 9-9.3 wherein the condition to
be treated or controlled is edema consequent to hypoxia, e.g.,
general systemic hypoxia, e.g., hypoxia caused by an interruption
of blood perfusion, for example wherein the edema is cerebral edema
consequent to hypoxia caused by cardiac arrest, stroke, or other
interruption of blood perfusion to the brain, or wherein the edema
is cardiac edema consequent to cardiac ischemia or other
interruption of blood flow to the heart. [0471] 9.23. Any of Uses
9-9.3 wherein the condition to be treated or controlled is cerebral
consequent to microgravity and/or radiation exposure, e.g.,
exposure from space flight or from working with radioactive
materials or from working in radioactive areas and/or optic nerve
edema, e.g., consequent to microgravity and/or radiation exposure,
e.g., exposure from space flight or from working with radioactive
materials or from working in radioactive areas, e.g., optic nerve
edema. [0472] 9.24. Any of Uses 9-9.3 wherein the condition to be
treated or controlled is cerebral edema consequent to invasive
central nervous system procedures, e.g., neurosurgery, endovascular
clot removal, spinal tap, aneurysm repair, or deep brain
stimulation. [0473] 9.25. Use 9.24 or 9.25 wherein the patient is
at elevated risk of edema, e.g., due to microgravity and/or
radiation exposure, neurosurgery, endovascular clot removal, spinal
tap, aneurysm repair, or deep brain stimulation. [0474] 9.26. Use
9.24 or 9.25 wherein the patient already has edema. [0475] 9.27.
Any of Uses 9, et seq. wherein the edema is cytotoxic cerebral
edema or is primarily cytotoxic cerebral edema. [0476] 9.28. Any of
Uses 9-9.17 or 9.22 wherein the edema is cytotoxic cerebral edema
or is primarily cytotoxic cerebral edema. [0477] 9.29. Any of Uses
9-9.2 wherein the condition to be treated or controlled is spinal
cord edema, e.g., spinal cord edema consequent to spinal cord
trauma, e.g., spinal cord compression. [0478] 9.30. Use 9.29
wherein the condition to be treated or controlled is spinal cord
edema consequent to spinal cord compression. [0479] 9.31. Any of
Uses 9-9.2 wherein the condition to be treated or controlled is
retinal edema. [0480] 9.32. Any of Uses 9-9.2 wherein the condition
to be treated or controlled is pulmonary edema. [0481] 9.33. Use 9
or 9.1 wherein the condition to be treated or controlled is
epilepsy. [0482] 9.34. Use 9 or 9.1 wherein the condition to be
treated or controlled is retinal ischemia or other diseases of the
eye associated with abnormalities in intraocular pressure and/or
tissue hydration. [0483] 9.35. Use 9 or 9.1 wherein the condition
to be treated or controlled is myocardial ischemia. [0484] 9.36.
Use 9 or 9.1 wherein the condition to be treated or controlled is
myocardial ischemia/reperfusion injury. [0485] 9.37. Use 9 or 9.1
wherein the condition to be treated or controlled is myocardial
infarction. [0486] 9.38. Use 9 or 9.1 wherein the condition to be
treated or controlled is myocardial hypoxia. [0487] 9.39. Use 9 or
9.1 wherein the condition to be treated or controlled is congestive
heart failure. [0488] 9.40. Use 9 or 9.1 wherein the condition to
be treated or controlled is sepsis. [0489] 9.41. Use 9 or 9.1
wherein the condition to be treated or controlled is a migraine.
[0490] 9.42. Use 9 or 9.1 wherein the condition to be treated or
controlled is glioblastoma. [0491] 9.43. Use 9 or 9.1 wherein the
condition to be treated or controlled is fibromyalgia. [0492] 9.44.
Use 9 or 9.1 wherein the condition to be treated or controlled is
multiple sclerosis. [0493] 9.45. Use 9 wherein the aquaporin is
AQP2. [0494] 9.46. Use 9 or 9.45 wherein the condition to be
treated is hyponatremia or excessive fluid retention, e.g.,
consequent to heart failure (HF), for example congestive heart
failure, liver cirrhosis, nephrotic disorder, syndrome of
inappropriate antidiuretic hormone secretion (SIADH), or
infertility treatment, e.g., infertility treatment. [0495] 9.47.
Use 9 or 9.45 wherein the condition to be treated is ovarian
hyperstimulation syndrome. [0496] 9.48. Use o or 9.45-9.47 further
comprising one or more of restriction of dietary sodium, fluid
and/or alcohol; and/or administration of one or more diuretics,
vasopressin receptor antagonists, angiotensin converting enzyme
(ACE) inhibitors, aldosterone inhibitors, angiotensin receptor
blockers (ARBs), beta-adrenergic antagonists (beta-blockers),
and/or digoxin. [0497] 9.49. Any of Use 9, et seq. wherein the
compound of Formula I or formula 1a inhibits aquaporin activity,
e.g., AQP2 and/or AQP4 activity, by at least 50% at concentrations
of 10 micromolar or less, for example inhibits APQ2 and/or AQP4
activity by at least 50% at concentrations of 10 micromolar or less
in an aquaporin-mediated cell volume change assay, e.g., is active
in any of the assays of Method 10, et seq. infra. [0498] 9.50. Any
of Use 9, et seq. wherein the duration of treatment with the
phenylbenzamide is less than 21 days, e.g., less than 2 weeks,
e.g., one week or less. [0499] 9.51. Any of Use 9, et seq. wherein
the medicament is formulated for oral administration. [0500] 9.52.
Any of Use 9, et seq. wherein the medicament is formulated for
parenteral administration. [0501] 9.53. Use 9.52 wherein the
medicament is formulated for intravenous administration.
[0502] A dose or method of administration of the dose of the
present invention is not particularly limited. Dosages employed in
practicing the present invention will of course vary depending,
e.g. on the particular disease or condition to be treated, the
particular compound used, the mode of administration, and the
therapy desired. The compounds may be administered by any suitable
route, including orally, parenterally, transdermally, or by
inhalation. In stroke or other severely debilitating diseases or
conditions, for example where the patient may be unconscious or
unable to swallow, an IV infusion or IV bolus may be preferred. In
general, satisfactory results, e.g. for the treatment of diseases
as hereinbefore set forth are indicated to be obtained on oral
administration at dosages of the order from about 0.01 to 15.0
mg/kg. In larger mammals, for example humans, an indicated daily
dosage for oral administration will accordingly be in the range of
from about 0.75 to 1000 mg per day, conveniently administered once,
or in divided doses 2 to 3 times, daily or in sustained release
form. Unit dosage forms for oral administration thus for example
may comprise from about 0.2 to 75 or 150 mg, e.g. from about 0.2 or
2.0 to 50, 75, 100, 125, 150 or 200 mg of a Compound of the
Invention, together with a pharmaceutically acceptable diluent or
carrier therefor. When the medicament is used via injection
(subcutaneously, intramuscularly or intravenously) the dose may be
0.25 to 500 mg per day by bolus or if IV by bolus or infusion.
[0503] Pharmaceutical compositions comprising compounds of Formula
I or formula 1a may be prepared using conventional diluents or
excipients and techniques known in the galenic art. Thus oral
dosage forms may include tablets, capsules, solutions, suspensions
and the like.
[0504] Methods of making and formulating compounds of Formula I or
formula 1a are set forth in US 2010/0274051 A1, U.S. Pat. No.
7,700,655, and in U.S. Pat. No. 7,626,042, each incorporated herein
by reference.
[0505] In a further embodiment, the invention provides a method,
e.g., Method 10, for identification of specific aquaporin
inhibitors, comprising measuring the response of an
aquaporin-expressing cell population versus a control cell
population to a hypertonic or hypotonic solution in the presence or
absence of a test compound. For example the invention provides,
e.g., [0506] 10. [0507] 10.1. Method 10 wherein the
aquaporin-expressing cell population expresses AQP2 or AQP4. [0508]
10.2. Any of Method 10 or 10.1 wherein the cells are mammalian,
e.g., transgenic CHO cells. [0509] 10.3. Any of Method 10, et seq.
wherein the control cells express a transgenic transmembrane
protein other than an aquaporin, e.g., CD81. [0510] 10.4. Any of
Method 10, et seq. wherein the cells are exposed to a hypotonic
environment for a period of time and at a concentration which
causes most of the aquaporin-expressing cell population to burst in
the absence of test compound, but not the control cell population,
e.g. 3-8 minutes in water. [0511] 10.5. Method 10.4 wherein cell
bursting is measured by a fluorescent signal that is produced by
viable cells but not by burst cells, e.g., conversion of
acetoxymethyl calcein (calcein-AM) to the fluorescent dye calcein.
[0512] 10.6. Method 10.4 or 10.5 wherein the cells are exposed to a
hypotonic environment, e.g., deionized water, for a period of 3-8
minutes, and then returned to normotonic environment (e.g. ca. 300
mOSM) then the proportion of viable cells is measured. [0513] 10.7.
Any of Method 10, et seq. wherein the measurement of viability is
the ability of the cells to convert acetoxymethyl calcein
(calcein-AM) to the fluorescent dye calcein. [0514] 10.8. Any of
the foregoing Methods 10.4, et seq. wherein a compound of Formula I
as hereinbefore described, e.g., of formula 1a, is used as a
positive control, which inhibits the aquaporin-expressing cell
population from bursting in a hypotonic environment. [0515] 10.9.
Any of the foregoing Methods 10.4-10.8 wherein a test compound is
identified as having aquaporin-inhibitory activity when the
aquaporin-expressing cell population is identified viable, e.g., by
the ability of the cells to convert acetoxymethyl calcein
(calcein-AM) to the fluorescent dye calcein, following an exposure
in a presence of test compound to a hypotonic environment that
renders the aquaporin-expressing cell population non-viable in the
absence of test compound. [0516] 10.10. Any of Method 10 or
10.1-10.3 wherein the cells are exposed to a hypertonic environment
for a period of time and at a concentration sufficient to cause the
aquaporin-expressing cell population to shrink in the absence of
test compound, e.g. 3-8 minutes at ca. 530 mOsm. [0517] 10.11.
Method 10.9 wherein the shrinkage of the cells is measured by light
scattering. [0518] 10.12. Any of Method 10.10, et seq. wherein the
hypertonic environment is approximately 530 mOsm and the normotonic
environment is approximately 300 mOsm. [0519] 10.13. Any of the
foregoing Methods 10.10, et seq. wherein a compound of Formula I as
hereinbefore described, e.g., of formula 1a, is used as a positive
control, which inhibits the aquaporin-expressing cell population
from shrinking in a hypertonic environment. [0520] 10.14. Any of
the foregoing Methods 10.10, et seq. wherein a test compound is
identified as inhibiting aquaporin activity by inhibiting the
aquaporin-expressing cell population from shrinking in a hypertonic
environment. [0521] 10.15. Any of the foregoing methods wherein a
test compound is identified as inhibiting aquaporin activity.
[0522] 10.16. Any of Method 10, et seq. wherein the
aquaporin-expressing cell population expresses AQP2. [0523] 10.17.
Any of Method 10, et seq. wherein the aquaporin-expressing cell
population expresses AQP4. [0524] 10.18. Any of Method 10, et seq.
wherein the test compound is a phenylbenzamide, e.g., of Formula I
as hereinbefore described, e.g., of formula 1a.
[0525] As used throughout, ranges are used as shorthand for
describing each and every value that is within the range. Any value
within the range can be selected as the terminus of the range. In
addition, all references cited herein are hereby incorporated by
referenced in their entireties. In the event of a conflict in a
definition in the present disclosure and that of a cited reference,
the present disclosure controls.
[0526] Unless otherwise specified, all percentages and amounts
expressed herein and elsewhere in the specification should be
understood to refer to percentages by weight. The amounts given are
based on the active weight of the material.
Example 1
Phenylbenzamide-AQP Structure-Activity Relationship
[0527] Structure activity relationships (SARs) are determined by
assaying analogues of selected hits to guide chemistry for the
preparation of new molecules to be tested for improved potency. For
this iterative process we use a quantitative kinetic assay--the
Aquaporin-Mediated Cell Volume Change Assa--in a 96-well multiplate
reader. It detects changes in light scattering by a monolayer of
CHO cells expressing the desired AQP as they shrink when exposed to
hypertonic solution (300 mOsm.fwdarw.530 mOsm). FIG. 1 depicts the
aquaporin-mediated cell volume change assay with AQP4 expressing
cells (FIG. 1A) and AQP2 expressing cells (FIG. 1B). The cells
expressing aquaporins shrink more rapidly than control cells, due
to enhanced water flow, which shrinkage can be inhibited by a
compound that inhibits the aquaporin.
[0528] In FIG. 1, aquaporin-expressing cells are shown in the
presence of DMSO (triangles) or in the presence of the test
compound (here, Compound 3) at 10 .mu.M (squares), along with
CHO-CD81 expressing control cells in the presence of DMSO
(diamonds). Each curve represents an average of 16 wells in the
96-well plate.
[0529] In FIG. 1A, when the AQP4b cells treated with DMSO are
exposed to hypertonic shock, the cells show rapid shrinking, giving
a rise in light scattering (increasing relative change in
absorbance, Abs/Abs.sub.0) followed by a decay as cells detach from
the plate. The CHO-AQP4b cell line shows a 4.5-fold increase in the
rate of shrinking compared to CHO-CD81 control cells (fitted to a
double exponential model). CHO-AQP4b cells treated with the
Compound 3 analogue at 10 .mu.M (squares) show a slower rate of
shrinking (55% inhibition) as seen by characteristic `unbending` of
the light scattering curve. Similarly, FIG. 1B depicts an
experiment comparing CHO-AQP2 treated with DMSO or with Compound 3
at 10 .mu.M. Aquaporin-2 has a lower intrinsic water permeability
than AQP4 as observed here. CHO-AQP2 cell lines treated with DMSO
(FIG. 1B, triangles) show a 1.7-fold increase in the rate of
shrinking compared to CHO-CD81 control cells (diamonds) also
treated with DMSO (fitted to a double exponential model) (FIG. 1B).
CHO-AQP2 cells treated with Compound 3 at 10 .mu.M (squares) show a
slower rate of shrinking (81% inhibition), when comparing the
relative change in Abs (Abs/Abs.sub.0) (FIG. 1B).
[0530] The data indicates that in this assay, Compound 3 is capable
of significantly inhibiting AQP2 and AQP4 activity, e.g. by greater
than 50%, at concentrations of 10 .mu.M.
Example 2
Aquaporin Specificity of the Phenylbenzamide Compounds
[0531] The specificity of the compounds is tested against the most
closely related of the 13 known aquaporins: AQP1, AQP2, AQP5 and
both splice variants of AQP4 (A and B). A stable CHO cell line is
created for each of the above aquaporins and the inhibition of
water permeability using the Aquaporin-Mediated Cell Volume Change
Assay with 10 .mu.M Compound 3 is tested. Compound 3 inhibits AQP2
and 4, while it poorly inhibits AQP1 and 5 (FIG. 2).
Example 3
Direct Drug-Target Interactions Between Phenylbenzamides and
AQP4
[0532] To support the mechanism of action by which phenylbenzamides
directly block AQP4, we perform in vitro binding studies using
purified AQP4b and Compound 4 radiolabeled with .sup.3H. Using a
Hummel-Dryer style assay, a gel filtration column is
equilibratrated with buffer containing detergent, to maintain
solubility of AQP4b, and 1 .mu.M [.sup.3H]-Compound 4. AQP4b is
diluted to 250 .mu.M in this column buffer and incubated at RT for
30 min. The sample is then applied to the column, fractions
collected and the presence of [.sup.3H]-Compound 4 detected by
liquid scintillation counting. FIG. 3 shows the elution profile of
[.sup.3H]-Compound 4 from the gel filtration column with the
elution positions of tetrameric and monomeric AQP4b indicated. The
rise in [.sup.3H]-Compound 4 from a baseline value of 1 .mu.M
represents binding to each of these proteins. Although no monomeric
AQP4b can be readily detected in our highly purified AQP4b by
conventional means, this assay reveals the presence of a small,
albeit vanishing, amount of monomer. The relative affinities for
Compound 4 are .about.100 .mu.M and less than 1 .mu.M for tetramer
and monomer, respectively. This assay shows relatively weak binding
of Compound 4 to solubilized AQP4b; nevertheless, it clearly
demonstrates that this phenylbenzamide directly interacts with
AQP4b.
Example 4
Pharmacological Proof-of-Concept
[0533] Mouse Water Toxicity Model--Survival Curves: The in vivo
efficacies of the compounds are tested using the mouse water
toxicity model, where a mouse is injected with water at 20% of its
body weight. Manley, G. T. et al. Aquaporin-4 deletion in mice
reduces brain edema after acute water intoxication and ischemic
stroke. Nat Med 6, 159-163 (2000); Gullans, S. R. & Verbalis,
J. G. Control of brain volume during hyperosmolar and hypoosmolar
conditions. Annual Review of Medicine 44, 289-301 (1993). The
resulting euvolemic hyponatremia rapidly leads to CE, making this a
practical model to test an inhibitor of the CNS aquaporin,
AQP4b.
[0534] The ability of mice to survive H.sub.2O toxicity is
determined in three experiments using 10-12 mice each (16-19 weak
old male/female). Deionized water is prepared for injection with
either 0.39 mg/kg phenylbenzamide (placebo) or 0.76 mg/kg with test
compound. FIG. 4 shows the combined results of these experiments
(n=33 placebo, n=34 Compound 1). Percent survival of the Compound 1
cohorts improves 3.2 fold and the time to 50% survival for animals
treated with Compound 1 is improved by roughly 52 min.
[0535] Mouse Water Toxicity Model--Brain Volume by Magnetic
Resonance Imaging (MRI): MRI is used to measure changes in brain
volume in response to water shock, using the water toxicity model.
As described for the survival and brain water content studies
above, mice are injected, IP, with a water bolus alone or water
bolus and test compound at 0.76 mg/kg, and changes in brain volume
as detected by MRI are monitored. Mouse brain volumes are assessed
using MRI scans collected with a 9.4 T Bruker Biospec MRI scanner
at the Case Center for Imaging Research at Case Western Reserve
University. This imaging method is found to provide sufficient
contrast and resolution to sensitively detect changes in total
brain volume in the mouse water toxicity model for cerebral edema.
High resolution T2-weighted sagittal scans (resolution=0.1
mm.times.0.1 mm.times.0.7 mm) of the mouse head are obtained prior
to water injection, 5.67 min post water injection, and then every
5.2 minutes until the animal expires from the water loading. Each
scan contains twenty-five 0.7 mm contiguous imaging slices of which
14-15 slices contain a portion of the brain. The cross sectional
area of the brain in each imaging slice is measured by manual
region-of-interest selection using ImageJ. Brain volumes are then
calculated for each scan by summing the individual cross sectional
brain areas and multiplying by the slice thickness (0.7 mm).
[0536] Treatment with Compound 1 at 0.76 mg/kg reduces the rate of
CE development from 0.081 to 0.032 min.sup.-1 (or 2.5-fold) fit to
a single exponential model (FIG. 5). Also, the extent of CE during
the period of observation is reduced (FIG. 5). Moreover, plasma
levels in the same assay are found to range between 0.03-0.06 .mu.g
as determined by LC-MS/MS (performed at Lerner Center, Cleveland
Clinic, Cleveland, Ohio) and are sufficient to show efficacy in
this model for CE.
[0537] The brain volume by magnetic resonance imaging experiment is
also conducted with phenylbenzamide (0.39 mg/kg) and Compound 4
(0.83 mg/kg). Compound 4 reduces the rate of CE development from
0.081 to 0.022 min.sup.-1 (Table 1). Phenylbenzamide fails to show
reduction in the rate of CE in mice (Table 1).
TABLE-US-00001 TABLE 1 Efficacy of compounds on CE formation in the
mouse water toxicity model AQP Inhibition Cerebral Edema Compound
Cell-Based Assay (%) Rate by MRI (min.sup.-1) No Drug 0 0.081
Compound 1 47.9 0.032 Phenylbenzamide 4.5 0.096 Compound 4 38.9
0.022 For no drug and Compound 1, n = 14 mice each. For
phenylbenzamide and Compound 4, n = 12 mice each.
Example 5
High Throughput Screening Assay
[0538] Under hypotonic shock, both untransfected cells and cells
expressing an unrelated transmembrane protein (CD81, at levels
equivalent to AQP4b) swell slowly but remain intact. These
observations are used to develop our high-throughput screening
assay (HTS).
[0539] After hypotonic shock in a 384 well plate format, we return
osmolality to normal (300 mOSM) by adding 2.times. concentrated
phosphate buffered saline supplemented to 2 .mu.M with a
nonfluorescent acetoxymethyl derivative of calcein (calcein-AM) to
each well. Intact cells take up calcein-AM and convert it to the
fluorescent dye calcein--giving a quantitative measure of the
remaining intact cells. Burst cells do not convert the precursor to
the dye. Water uptake by AQP4-expressing cells is relatively rapid,
with most test cells bursting within 4 min of hypotonic shock,
whereas most cells expressing CD81 remain viable after 8 min.
Intracellular conversion of calcein-AM provides a strong and easily
detectable signal at 535 nM in our assay (FIG. 6).
[0540] Calcein Fluorescence End-Point Assay:
[0541] Cells are seeded 24 hr before assay to reach 100%
confluence. Culture medium is replaced with H.sub.2O for 5:30 min
(osmotic shock). Osmolality is then normalized with the addition of
2.times.PBS plus 2 .mu.M calcein-AM. Cells are then incubated at
37.degree. C. for an additional 30 min and fluorescence measured on
a plate-reader. Rows 1-22 are seeded with CHO-AQP4 cells, and rows
23-24, with CHO-CD81 cells (384 well plate). Note, all plate edges
are discarded. Relative Fluorescence Intensity is calculated as the
fluorescence intensity (FI) of each well divided by the mean FI of
AQP4 cells treated with DMSO (control). Criteria for a successful
assay: coefficients of variation (CVs) <15%, and Z-factors
>0.5. Statistical analysis shows that 5.5 min of osmotic shock
provides the optimal signal-to-noise ratio.
TABLE-US-00002 TABLE 2 Statistics for endpoint `calcein` assay in
FIG. 6; 5:30 min time point shown: Mean StDev CV Z' S/B AQP4 581618
66311 11% 0.629 5.0 CD81 2910106 221240 8%
[0542] As will be observed, the signal for the CD81 cells is ca.
5.times. higher than the signal for the APQ4 cells, because by 5.5
mins, most of the AQP4 cells have burst, while most of the CD81
cells remain intact. Inhibition of AQP4 would therefore be expected
to provide a higher signal, more like the CD81 cells.
[0543] This assay is applied in a pilot screen of the MicroSource
GenPlus 960 and the Maybridge Diversity.TM. 20 k libraries
(approximately 21,000 compounds tested, each compound at 10-20
.mu.M).
[0544] From this assay, a specific chemical series is identified,
phenylbenzamides, which represents 3 out of the top 234 hits.
[0545] Hits from the HTS are validated using the same assay using a
different plating arrangement. In FIG. 7, we show this validation
assay used to examine Compound 3. Cells are seeded in a 96 well
multiplate format with the plates edges omitted (lanes 1 and 24)
and an entire column (n=16) is used to test the ability of a
compound to block AQP4-mediated cell bursting upon H.sub.2O shock.
CHO cells expressing CD81 are seeded in lanes 2-3 as a control, and
CHO cells expressing AQP4, in lanes 4-23. Cells are treated with
0.1% DMSO in 10% FBS, DMEM (even numbered columns) or 10 .mu.M
Compound 1 (odd number columns) in 0.1% DMSO, 10% FBS, DMEM for 30
minutes. The cells are shocked with H.sub.2O for 5:30 minutes, then
osmolality returned to 300 mOSM in the presence of 1 .mu.M
calcein-AM, as described above. The cells are incubated at
37.degree. C. for 30 minutes and the relative fluorescence measured
(ex 495/em 535 nM) on a fluoresence multiplate reader. The data in
FIG. 7 represents the average relative fluorescence units
(RFU.+-.SEM, n=16).
Example 6
Water Toxicity Model for CE: Intracranial Pressure (ICP)
[0546] ICP is monitored using a Samba 420 Sensor, pressure
transducer, with a Samba 202 control unit (Harvard Apparatus,
Holliston, Mass.). This ICP monitoring system consists of a 0.42 mm
silicon sensor element mounted on an optical fiber. A 20-gauge
syringe needle is implanted through the cisterna magna to a depth
of .about.1 cm. The needle then acts as a guide for insertion of
the Samba Sensor and the site of implantation and the open end of
the needle are sealed with 100% silicone sealant. A baseline ICP
reading is established followed by a water bolus IP injection (20%
weight of animal) with or without Compound 1. ICP is monitored
until the animal expires from the water load.
[0547] Adjusting for the slight rise in ICP observed in the animals
when they are monitored without the water bolus injection (FIG. 8,
No Water Toxicity), Compound 1 at 0.76 mg/kg reduces the relative
rate of ICP rise by 36%, from 3.6.times.10.sup.-3 min.sup.-1 to
2.3.times.10.sup.-3 min.sup.-1 (n=6 mice/treatment,
mean.+-.SEM).
Example 7
Conversion of
2-((3,5-bis(trifluoromethyl)phenyl)carbamoyl)-4-chlorophenyl
dihydrogen phosphate bis ethanolamine salt to Compound 1
[0548] Plasma or serum levels of Compound 1 are measured by
LC-MS/MS at the Mass Spectrometry II Core facility at the Lerner
Research Institute of the Cleveland Clinic Foundation. Measurements
are taken at 15 minutes and 24 hours after a 10 mg/kg i.p. loading
dose and 1 mg/ml at 8 .mu.l/h maintenance dose (delivered by an
Alzet i.p. osmotic pump, Durect Corp., Cupertino, Calif.) of
2-((3,5-bis(trifluoromethyl)phenyl)carbamoyl)-4-chlorophenyl
dihydrogen phosphate bis ethanolamine salt (n=5 mice/time point,
mean.+-.SEM) (FIG. 9). After initial processing to remove proteins
(75% acetonitrile extraction), Compound 3 is introduced to improve
quantitation using multiple reaction monitoring (MRM). Samples are
analyzed by tandem LC-MS/MS using C18 reversed-phase chromatography
and mass analysis with a triple-quadrapole mass spectrometer. The
LC method is sufficient to separate Compound 1 from Compound 3 and
subsequent MRM gave reliable quantitation with a linear response
from 0.004-0.4 ng of Compound 1 for its most abundant daughter ion.
The dashed line in FIG. 9 is the relative effective plasma
concentration of Compound 1 observed in the mouse water toxicity
model. Inclusion of an Alzet osmotic pump (Durect Corp., Cupertino,
Calif.) containing
2-((3,5-bis(trifluoromethyl)phenyl)carbamoyl)-4-chlorophenyl
dihydrogen phosphate bis ethanolamine salt in the peritoneum is
sufficient, in conjunction with an initial loading dose, to sustain
Compound 1 above the expected efficacious plasma concentration of
20 ng/ml for 24 hours (FIG. 9).
[0549] The solubility of Compound 1 in water is 3.8 .mu.g/ml. The
solubility of Compound 5 in water is 1 mg/ml.
[0550] Initial experiments show rapid bioconversion of
2-((3,5-bis(trifluoromethyl)phenyl)carbamoyl)-4-chlorophenyl
dihydrogen phosphate bis ethanolamine salt to Compound 1 when added
to mouse plasma in vitro. Less than 5 minutes at 20.degree. C. is
sufficient to render
2-((3,5-bis(trifluoromethyl)phenyl)carbamoyl)-4-chlorophenyl
dihydrogen phosphate bis ethanolamine salt undetectable. In
addition,
2-((3,5-bis(trifluoromethyl)phenyl)carbamoyl)-4-chlorophenyl
dihydrogen phosphate bis ethanolamine salt is undetectable in
plasma samples taken from mice injected IP with
2-((3,5-bis(trifluoromethyl)phenyl)carbamoyl)-4-chlorophenyl
dihydrogen phosphate bis ethanolamine salt. Instead, Compound 1 is
detected at a concentration consistent with good bioavailability
and near-complete conversion of
2-((3,5-bis(trifluoromethyl)phenyl)carbamoyl)-4-chlorophenyl
dihydrogen phosphate bis ethanolamine salt. With
2-((3,5-bis(trifluoromethyl)phenyl)carbamoyl)-4-chlorophenyl
dihydrogen phosphate bis ethanolamine salt, doses of 10 mg/kg and
IP injection volumes in saline (0.5 ml for a 30 g mouse), that give
serum concentrations of Compound 1 in excess of 400 ng/ml (FIG. 9)
can be used. Key PK parameters in mice are: rate of absorption 0.12
min.sup.-1; rate of elimination 0.017 min.sup.-1.
Example 8
Animal Stroke Model
[0551] Most ischemic strokes 80%) occur in the region of the middle
cerebral artery (MCA). To mimic this injury in mice, an
intraluminal monofilament model of middle cerebral artery occlusion
(MCAo) is used. Occlusion is achieved by inserting a surgical
filament into the external carotid artery (ECA) and threading it
forward into the internal carotid artery (ICA) until the tip blocks
the origin of the MCA. The resulting cessation of blood flow gives
rise to subsequent brain infarction in the MCA territory (Longa, E.
Z. et al., Reversible Middle Cerebral Artery Occlusion Without
Craniectomy in Rats, Stroke, 20, 84-91 (1989)). This technique is
used to study a temporary occlusion in which the MCA is blocked for
one hour. The filament is then removed allowing reperfusion to
occur for 24 hours before the animal's brain was imaged using
T2-weighted scans in a 9.4 T Bruker MRI scanner at the Case Center
for Imaging Research (FIG. 10). FIG. 10 shows a single slice from a
T2-weighted MR image depicting the center of the brain showing
cerebral cortex, hippocampus, thalamus, amygdala and hypothalamus
for a "Normal" mouse (left panels) and a mouse which receives MCAo
for one hour followed by 24 hours of reperfusion (right panels).
Dashed lines mark the midline of the brain and show a large shift
in the MCAo brain due to cerebral edema. Solid line highlights the
region of infarct in the MCAo brain.
[0552] Survival--
[0553] Mice are treated with Compound 5 using a 2 mg/kg i.p.
loading dose and 1 mg/ml at 8 .mu.l/h maintenance dose (delivered
by an i.p. osmotic pump) of Compound 5, or given saline (controls;
n=17) using an identical approach. In this model, we observed a
29.4% improvement in overall survival at 24 h when animals are
treated with Compound 5 (X.sup.2(1)=4.26; P<0.05).
[0554] Cerebral Edema--
[0555] Mice are given saline or treated with Compound 5 by
multi-dosing at 5 mg/kg i.p. every three hours (n=8 per treatment).
This dosing regimen is sufficient to maintain a plasma
concentration of Compound 1 >20 ng/ml for the duration of the
study. Ipsilateral and contralateral hemispheric volume is measured
from the T2-weighted MR images of mice 24 hours post-icus. Relative
change in hemispheric volume is calculated as a percent of the
difference between ipsilateral brain volume (V.sub.i) and
contralateral brain volume (V.sub.c) relative to the contralateral
brain volume (Percent Change in Hemispheric Brain
Volume=((V.sub.i-V.sub.c)/V.sub.c).times.100%.
[0556] Control animals show swelling in the ipsilateral hemisphere
with a relative change in ipsilateral brain volume of
13.4%.+-.1.9%, while animals given Compound 5 show a 4.2.+-.1.7%
change (P=0.003, .+-.SEM, see FIG. 11). This represents a 3.2-fold
reduction in brain swelling after MCAo.
[0557] Neurological Outcome--
[0558] In the same experiment as above, animals are scored for
neurological outcome on a simple 5 point scale described in Manley,
G. T. et al., Aquaporin-4 Deletion in Mice Reduces Brain Edema
After Acute Water Intoxication and Ischemic Stroke, Nature
Medicine, 6, 159-163 (2000). An improvement in neurological outcome
is observed for animals given Compound 5. Control animals have an
average neurological score of 2.77.+-.0.66, while animals given
Compound 5 have an average score of 0.88.+-.0.31 (FIG. 13, inset,
P=0.025, n=9 per treatment). Animals given Compound 5 did not
progress into a state of severe paralysis or death.
[0559] The data from the MCAo stroke model together with the water
toxicity (brain edema) model link the pharmacology of Compound
5/Compound 1 with improved outcomes in stroke.
* * * * *